Ligand source activities (1 row/activity)





Ligands Receptor Assay information Chemical information
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name
GPCRdb ID #Vendors Reference
ligand
Fold selectivity
(Potency)
# tested GPCRs
(Potency)
Species p-value
(-log)
Type Activity
Relation
Activity
Value
Assay Type Assay Description Source Mol
weight
Rot
Bonds
H don H acc LogP Smiles DOI
CHEMBL1627325 215590 0 None 1 8 Human 10.5 pEC50 = 10.5 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None CSCC[C@H](NC(=O)CNC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](N)CO)C(C)(C)C)C(C)C)[C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)O)[C@@H](C)O 10.1021/jm900604g
3812 7504 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
439201 7504 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
649 7504 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
CHEMBL406291 7504 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
DB12126 7504 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
9851817 16453 0 None - 1 Guinea pig 7.0 pEC50 = 7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 16453 0 None - 1 Guinea pig 7.0 pEC50 = 7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44340964 16479 0 None - 1 Guinea pig 6.0 pEC50 = 6.0 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 16479 0 None - 1 Guinea pig 6.0 pEC50 = 6.0 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44341039 16283 0 None - 1 Guinea pig 6.9 pEC50 = 6.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 16283 0 None - 1 Guinea pig 6.9 pEC50 = 6.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44340818 117386 0 None - 1 Guinea pig 5.9 pEC50 = 5.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 117386 0 None - 1 Guinea pig 5.9 pEC50 = 5.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
18941161 16501 0 None - 1 Guinea pig 4.7 pEC50 = 4.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 16501 0 None - 1 Guinea pig 4.7 pEC50 = 4.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
44341214 117207 0 None - 1 Guinea pig 6.7 pEC50 = 6.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 117207 0 None - 1 Guinea pig 6.7 pEC50 = 6.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
18941160 16687 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 16687 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
44214279 16488 0 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 16488 0 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
10895913 16641 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 16641 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
9831859 16478 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 16478 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10257108 16603 1 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 16603 1 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
44340760 117285 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 117285 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
22008916 16534 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 16534 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44214619 117382 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 117382 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
18941145 16735 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 16735 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
22008929 16522 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 16522 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
22008895 117335 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 117335 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
44340859 16815 0 None - 1 Guinea pig 7.2 pEC50 = 7.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 16815 0 None - 1 Guinea pig 7.2 pEC50 = 7.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44340951 16774 0 None - 1 Guinea pig 6.2 pEC50 = 6.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 16774 0 None - 1 Guinea pig 6.2 pEC50 = 6.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
3812 7504 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
439201 7504 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
649 7504 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
CHEMBL406291 7504 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
DB12126 7504 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
CHEMBL2372138 216968 0 None - 1 Human 8.0 pED50 = 8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None [N-]=[N+]=Nc1ccc(C[C@H](NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C(=O)N[C@@H](CO)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372165 216972 0 None - 1 Human 7.7 pED50 = 7.7 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccc(N)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372173 216975 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc([N+](=O)[O-])cc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372157 216970 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None N#[N+]c1ccc(C[C@H](NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372164 216971 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None N#[N+]c1ccc(C[C@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372172 216974 0 None - 1 Human 7.2 pED50 = 7.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(N)cc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372156 216969 0 None - 1 Human 8.2 pED50 = 8.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccc([N+](=O)[O-])cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372168 216973 0 None - 1 Human 8.2 pED50 = 8.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None [N-]=[N+]=Nc1ccc(C[C@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
44191040 202763 0 None - 1 Human 9.3 pIC50 = 9.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559825 202763 0 None - 1 Human 9.3 pIC50 = 9.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
667 8754 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
6918173 8754 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
71364 8754 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
CHEMBL2028850 8754 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
DB06196 8754 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
25019714 203362 2 None - 1 Human 9.0 pIC50 = 9.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL563956 203362 2 None - 1 Human 9.0 pIC50 = 9.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
45272156 201838 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL549534 201838 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190944 202712 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559436 202712 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190263 202733 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
CHEMBL559565 202733 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
10327403 85360 0 None 1 2 Rat 8.7 pIC50 = 8.7 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 85360 0 None 1 2 Rat 8.7 pIC50 = 8.7 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9987299 85376 0 None 2 2 Rat 7.0 pIC50 = 7.0 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 85376 0 None 2 2 Rat 7.0 pIC50 = 7.0 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190941 202210 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
CHEMBL552296 202210 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
10327403 85360 0 None -1 2 Human 7.9 pIC50 = 7.9 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 85360 0 None -1 2 Human 7.9 pIC50 = 7.9 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190852 202185 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552090 202185 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
44191220 201809 0 None - 1 Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL549337 201809 0 None - 1 Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2370243 216591 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None N=C(N)NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)c1ccc(CN2CCCNCCNCCCNCC2)cc1)c1cccs1)C(=O)O 10.1021/jm00015a001
10327403 85360 0 None 1 2 Rat 6.9 pIC50 = 6.9 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 85360 0 None 1 2 Rat 6.9 pIC50 = 6.9 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190672 202123 0 None - 1 Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551757 202123 0 None - 1 Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
9987299 85376 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 85376 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44189787 203123 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562434 203123 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190853 203068 4 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
CHEMBL562097 203068 4 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
44190850 202002 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL550827 202002 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
9987299 85376 0 None 2 2 Rat 8.6 pIC50 = 8.6 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 85376 0 None 2 2 Rat 8.6 pIC50 = 8.6 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190851 203349 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563878 203349 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
44190854 202224 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL552384 202224 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
44190753 203482 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL564841 203482 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190077 203249 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563254 203249 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190266 202235 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL552442 202235 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191138 202695 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559273 202695 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190943 202732 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
CHEMBL559564 202732 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
45267862 203099 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL562296 203099 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
44190751 202124 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 202124 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
44190942 203006 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
CHEMBL561634 203006 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
44190581 202723 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL559506 202723 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
44190267 201915 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550143 201915 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190168 201897 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550016 201897 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191224 203040 0 None - 1 Human 5.5 pIC50 = 5.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561839 203040 0 None - 1 Human 5.5 pIC50 = 5.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191226 202081 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551435 202081 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190361 201582 0 None - 1 Human 5.4 pIC50 = 5.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL538865 201582 0 None - 1 Human 5.4 pIC50 = 5.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44189789 202932 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561223 202932 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190167 203268 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563391 203268 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44189792 201914 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550142 201914 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190752 202125 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
CHEMBL551759 202125 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
44190165 202742 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559645 202742 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
667 8754 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
6918173 8754 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
71364 8754 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
CHEMBL2028850 8754 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
DB06196 8754 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
10327403 85360 0 None -1 2 Human 7.3 pIC50 = 7.3 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 85360 0 None -1 2 Human 7.3 pIC50 = 7.3 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44189790 203421 0 None - 1 Human 5.2 pIC50 = 5.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564341 203421 0 None - 1 Human 5.2 pIC50 = 5.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190166 203413 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564294 203413 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190269 202975 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561415 202975 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190756 202216 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552359 202216 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190268 203290 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563516 203290 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190754 203227 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563068 203227 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
44191223 203046 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561899 203046 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2370243 216591 0 None - 1 Guinea pig 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None N=C(N)NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)c1ccc(CN2CCCNCCNCCCNCC2)cc1)c1cccs1)C(=O)O 10.1021/jm00015a001
9987299 85376 0 None -2 2 Human 7.0 pIC50 = 7.0 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 85376 0 None -2 2 Human 7.0 pIC50 = 7.0 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190755 202606 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL558279 202606 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
44191225 203175 0 None - 1 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562747 203175 0 None - 1 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10463883 90608 0 None - 0 Guinea pig 10.4 pKd = 10.4 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 90608 0 None - 0 Guinea pig 10.4 pKd = 10.4 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
11498853 89963 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL218427 89963 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL541758 89963 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 89963 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218427 89963 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL541758 89963 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
57345657 78367 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 78367 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 78367 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 82701 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 82701 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10373970 144392 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 144392 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 144409 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 144409 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10101294 146932 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 146932 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
57403503 78440 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956856 78440 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963651 78440 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105746 168709 0 None - 0 Human 9.8 pKd = 9.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415366 168709 0 None - 0 Human 9.8 pKd = 9.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
9988753 90607 0 None - 0 Guinea pig 9.8 pKd = 9.8 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 90607 0 None - 0 Guinea pig 9.8 pKd = 9.8 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10010104 148052 0 None - 0 Guinea pig 9.7 pKd = 9.7 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 148052 0 None - 0 Guinea pig 9.7 pKd = 9.7 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
16105703 143258 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373607 143258 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
10373970 144392 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 144392 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44378635 175526 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL 1351 29 15 18 -2.0 C[C@@]12CCCC[C@]1(C)N(C(=O)[C@H]1Cc3ccccc3CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)c1ccc(NC(N)C=N)cc1)[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2 10.1016/S0960-894X(01)80847-7
CHEMBL437155 175526 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL 1351 29 15 18 -2.0 C[C@@]12CCCC[C@]1(C)N(C(=O)[C@H]1Cc3ccccc3CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)c1ccc(NC(N)C=N)cc1)[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2 10.1016/S0960-894X(01)80847-7
667 8754 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
6918173 8754 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
71364 8754 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
CHEMBL2028850 8754 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
DB06196 8754 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
57345657 78367 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 78367 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 78367 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11600324 148774 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL387452 148774 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44412007 83986 1 None - 0 Guinea pig 9.5 pKd = 9.5 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 83986 1 None - 0 Guinea pig 9.5 pKd = 9.5 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
667 8754 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
6918173 8754 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
71364 8754 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
CHEMBL2028850 8754 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
DB06196 8754 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
57399983 78350 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956859 78350 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963149 78350 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401772 78363 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956857 78363 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963175 78363 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
44412007 83986 1 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 83986 1 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
57401770 78358 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956853 78358 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963162 78358 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396534 78439 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956854 78439 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963650 78439 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL3038099 217711 0 None - 0 Rat 9.3 pKd = 9.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10079793 100895 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL249235 100895 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105698 143124 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373459 143124 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079797 144375 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375576 144375 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105734 91047 0 None - 0 Human 9.2 pKd = 9.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221285 91047 0 None - 0 Human 9.2 pKd = 9.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
57394782 78418 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956855 78418 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963557 78418 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10101294 146932 0 None - 0 Human 9.1 pKd = 9.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380273 146932 0 None - 0 Human 9.1 pKd = 9.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
57399228 78347 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956720 78347 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963146 78347 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57402746 78348 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956721 78348 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963147 78348 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401778 78353 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956870 78353 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963152 78353 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57400986 78357 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956723 78357 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963161 78357 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
9988753 90607 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 90607 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10418701 103877 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL267493 103877 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 144409 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 144409 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10101294 146932 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 146932 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038100 217712 0 None - 0 Rat 9.1 pKd = 9.1 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None N=C(N)NCCCCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
667 8754 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
6918173 8754 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
71364 8754 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
CHEMBL2028850 8754 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
DB06196 8754 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
57396538 78364 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956861 78364 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963176 78364 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394780 78417 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956852 78417 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963556 78417 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105751 90004 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL218636 90004 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
16105690 90409 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220478 90409 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105729 143712 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374273 143712 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038095 217708 0 None - 0 Rat 8.9 pKd = 8.9 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
CHEMBL2371961 216937 0 None - 0 Guinea pig 8.8 pKd = 8.8 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00069a016
57401776 78351 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956866 78351 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963150 78351 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401782 78361 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956873 78361 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963165 78361 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10463883 90608 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 90608 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105701 90744 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220693 90744 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
10441167 103763 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL266493 103763 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102701 144216 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375354 144216 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105694 148672 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL386794 148672 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9897921 168680 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415151 168680 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2372283 216988 0 None - 0 Rat 8.8 pKd = 8.8 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57398324 78360 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956862 78360 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963164 78360 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105727 90586 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220591 90586 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10396101 91117 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221683 91117 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441194 91397 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222156 91397 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105742 144932 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL376866 144932 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10418495 84650 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209346 84650 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
44354187 123578 0 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 29 11 10 0.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@@H](C(=O)O)C[C@H]2CCCC[C@H]21)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL337833 123578 0 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 29 11 10 0.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@@H](C(=O)O)C[C@H]2CCCC[C@H]21)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL410363 219595 24 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
10010669 83586 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206938 83586 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
70685700 81278 0 None - 0 Rabbit 6.9 pKd = 6.9 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 670 6 6 6 0.7 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2028840 81278 0 None - 0 Rabbit 6.9 pKd = 6.9 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 670 6 6 6 0.7 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2370040 216552 0 None - 0 Guinea pig 7.9 pKd = 7.9 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None C[C@@](Cc1ccccc1)(NC(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44354059 123837 0 None - 0 Guinea pig 5.9 pKd = 5.9 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 34 11 10 1.8 CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
CHEMBL339159 123837 0 None - 0 Guinea pig 5.9 pKd = 5.9 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 34 11 10 1.8 CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
CHEMBL3038103 217715 0 None - 1 Rat 5.9 pKd = 5.9 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1)C1CCCC1 10.1021/jm950716i
70685699 81272 0 None - 0 Rabbit 6.8 pKd = 6.8 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 747 10 6 9 1.1 NCCCC[C@@H]1N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)NC1=O 10.1021/jm950682e
CHEMBL2028835 81272 0 None - 0 Rabbit 6.8 pKd = 6.8 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 747 10 6 9 1.1 NCCCC[C@@H]1N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)NC1=O 10.1021/jm950682e
CHEMBL3038104 217716 0 None - 1 Rat 6.8 pKd = 6.8 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL3038096 217709 0 None - 1 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10056816 84524 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209038 84524 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
11513471 145425 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
CHEMBL377612 145425 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
56668285 70092 0 None - 0 Guinea pig 5.7 pKd = 5.7 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1145 26 13 15 -1.1 C=C([C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)CC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
CHEMBL1793829 70092 0 None - 0 Guinea pig 5.7 pKd = 5.7 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1145 26 13 15 -1.1 C=C([C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)CC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
10439868 82701 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL205093 82701 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
11600186 85072 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210788 85072 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10418252 145669 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378237 145669 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
57401774 78368 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956863 78368 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963184 78368 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391279 78369 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956876 78369 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963185 78369 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401784 78414 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956875 78414 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963532 78414 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57392147 78444 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1955876 78444 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963660 78444 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 82701 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 82701 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
16105696 89983 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218540 89983 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
57403505 78420 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956865 78420 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963559 78420 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL3038101 217713 0 None - 0 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
CHEMBL3038105 217717 0 None - 1 Rat 5.7 pKd = 5.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)O)Cc1ccccc1 10.1021/jm950716i
70696204 81273 0 None - 0 Rabbit 6.7 pKd = 6.7 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 690 6 4 7 0.9 CN1CC(=O)N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C1=O 10.1021/jm950682e
CHEMBL2028836 81273 0 None - 0 Rabbit 6.7 pKd = 6.7 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 690 6 4 7 0.9 CN1CC(=O)N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C1=O 10.1021/jm950682e
CHEMBL2372278 216986 0 None - 0 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None N=C(N)NCCCCC(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL2370010 216546 0 None - 0 Guinea pig 6.6 pKd = 6.6 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N1)C(=O)O 10.1021/jm00069a016
70687850 81279 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 594 4 5 6 -0.7 C[C@@H]1NC(=O)CNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028841 81279 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 594 4 5 6 -0.7 C[C@@H]1NC(=O)CNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
11506007 84786 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209773 84786 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
10463758 145649 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378189 145649 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
90662813 113344 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 722 15 6 8 1.3 NCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142191 113344 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 722 15 6 8 1.3 NCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2370042 216554 0 None - 0 Guinea pig 5.6 pKd = 5.6 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None CN(C(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44410425 103914 0 None - 0 Human 5.6 pKd = 5.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL267822 103914 0 None - 0 Human 5.6 pKd = 5.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
10010104 148052 0 None - 0 Human 8.5 pKd = 8.5 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383167 148052 0 None - 0 Human 8.5 pKd = 8.5 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
57396536 78359 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956860 78359 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963163 78359 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57393060 78362 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956851 78362 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963174 78362 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398326 78419 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956864 78419 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963558 78419 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11766718 143711 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374272 143711 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10010104 148052 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 148052 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038094 217707 0 None - 0 Rat 8.5 pKd = 8.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCC1 10.1021/jm950716i
CHEMBL3038106 217718 0 None - 0 Rat 8.5 pKd = 8.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1C[C@@H](O)C[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57401780 78354 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956872 78354 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963153 78354 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398328 78443 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956874 78443 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963659 78443 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
90662795 113341 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 778 17 9 8 1.4 N=C(N)NCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142173 113341 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 778 17 9 8 1.4 N=C(N)NCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
70681476 81281 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 709 5 7 8 -1.5 C[C@@H]1NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC1=O 10.1021/jm950682e
CHEMBL2028844 81281 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 709 5 7 8 -1.5 C[C@@H]1NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC1=O 10.1021/jm950682e
44354175 103683 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1025 35 12 12 0.8 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H]2CCCC[C@H]2C[C@@H]1C(=O)O)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL265814 103683 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1025 35 12 12 0.8 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H]2CCCC[C@H]2C[C@@H]1C(=O)O)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL2370700 216695 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21)C1Cc2ccccc2C1)C1Cc2ccccc2C1 10.1021/jm980495r
70696205 81276 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 704 6 6 7 1.5 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028839 81276 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 704 6 6 7 1.5 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
90662796 113342 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 792 18 9 8 1.8 N=C(N)NCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142174 113342 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 792 18 9 8 1.8 N=C(N)NCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
90662812 113343 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 716 15 6 7 1.2 NCCCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142190 113343 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 716 15 6 7 1.2 NCCCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
11527838 85133 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL211017 85133 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10008626 145456 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377800 145456 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10463818 146050 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379063 146050 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10102599 148182 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383989 148182 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44354176 103530 0 None - 0 Guinea pig 5.4 pKd = 5.4 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 28 10 10 0.6 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
CHEMBL264517 103530 0 None - 0 Guinea pig 5.4 pKd = 5.4 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 28 10 10 0.6 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
10032469 81275 0 None - 0 Rabbit 7.4 pKd = 7.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 676 6 6 7 0.8 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2028838 81275 0 None - 0 Rabbit 7.4 pKd = 7.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 676 6 6 7 0.8 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CNC1=O 10.1021/jm950682e
70696206 81284 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 797 5 7 8 0.2 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028847 81284 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 797 5 7 8 0.2 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)CCCNC1=O 10.1021/jm950682e
70696207 81286 0 None - 0 Rabbit 7.3 pKd = 7.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 791 7 8 9 0.0 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028849 81286 0 None - 0 Rabbit 7.3 pKd = 7.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 791 7 8 9 0.0 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
90662814 113345 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 806 21 6 8 3.6 NCCCCCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142192 113345 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 806 21 6 8 3.6 NCCCCCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
70694084 81280 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 808 6 7 7 1.3 C[C@@H]1NC(=O)[C@H](Cc2cc3ccccc3[nH]2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028843 81280 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 808 6 7 7 1.3 C[C@@H]1NC(=O)[C@H](Cc2cc3ccccc3[nH]2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
57396540 78365 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956867 78365 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963177 78365 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394784 78442 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956871 78442 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963658 78442 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10350966 91399 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222167 91399 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102296 168681 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415152 168681 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038102 217714 0 None - 0 Rat 7.3 pKd = 7.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)Cc1ccccc1 10.1021/jm950716i
CHEMBL2370011 216547 0 None - 0 Guinea pig 6.3 pKd = 6.3 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N[C@@H](Cc2ccccc2)C(=O)N1)C(=O)O 10.1021/jm00069a016
CHEMBL2372276 216985 0 None - 1 Rat 7.3 pKd = 7.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950716i
70694085 81283 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 771 6 8 8 0.1 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](c2ccccc2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028846 81283 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 771 6 8 8 0.1 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](c2ccccc2)NC(=O)CCCNC1=O 10.1021/jm950682e
10441297 143666 0 None - 0 Human 8.2 pKd = 8.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374224 143666 0 None - 0 Human 8.2 pKd = 8.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2370699 216694 7 None - 0 Guinea pig 8.2 pKd = 8.2 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
70681477 81282 0 None - 0 Rabbit 7.2 pKd = 7.2 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 6 6 8 0.8 C[C@@H]1NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028845 81282 0 None - 0 Rabbit 7.2 pKd = 7.2 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 6 6 8 0.8 C[C@@H]1NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
10349694 83358 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206312 83358 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10055774 83478 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206474 83478 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10260476 84772 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209719 84772 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL2372276 216985 0 None - 1 Rabbit 5.1 pKd = 5.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
70692045 81274 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 10 9 8 0.4 N=C(N)NCCC[C@@H]1NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
CHEMBL2028837 81274 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 10 9 8 0.4 N=C(N)NCCC[C@@H]1NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
70689879 81285 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 777 7 7 9 -0.6 C[C@@H]1NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
CHEMBL2028848 81285 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 777 7 7 9 -0.6 C[C@@H]1NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
44354174 148337 0 None - 0 Guinea pig 6.1 pKd = 6.1 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1081 35 14 12 -1.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
CHEMBL384846 148337 0 None - 0 Guinea pig 6.1 pKd = 6.1 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1081 35 14 12 -1.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
73345363 96116 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 793 17 8 9 -0.1 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2369364 96116 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 793 17 8 9 -0.1 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
73354461 96127 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 688 13 6 7 0.4 NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2369400 96127 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 688 13 6 7 0.4 NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
73354460 96125 0 None - 0 Rabbit 6.0 pKd = 6.0 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 718 14 7 8 -0.2 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1ccccc1)C(=O)O 10.1021/jm950682e
CHEMBL2369392 96125 0 None - 0 Rabbit 6.0 pKd = 6.0 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 718 14 7 8 -0.2 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1ccccc1)C(=O)O 10.1021/jm950682e
119343 9649 22 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
676 9649 22 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
CHEMBL446325 9649 22 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
653 7353 0 None 5 3 Human 8.4 pA2 = 8.4 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
5311108 8467 18 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
674 8467 18 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
CHEMBL130517 8467 18 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
667 8754 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
6918173 8754 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
71364 8754 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
CHEMBL2028850 8754 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
DB06196 8754 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
5128451 8162 0 None -1 2 Human 5.1 pIC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
646 8162 0 None -1 2 Human 5.1 pIC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
5128451 8162 0 None 1 2 Mouse 5.2 pIC50 = 5.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
646 8162 0 None 1 2 Mouse 5.2 pIC50 = 5.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
672 9047 21 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
6918284 9047 21 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
CHEMBL2105864 9047 21 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
DB06549 9047 21 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
5311108 8467 18 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
674 8467 18 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
CHEMBL130517 8467 18 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
3812 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3812 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
439201 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
439201 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
649 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
649 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
CHEMBL406291 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL406291 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
DB12126 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB12126 7504 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
667 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
667 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
6918173 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
6918173 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
71364 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
71364 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
CHEMBL2028850 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL2028850 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
DB06196 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB06196 8754 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
10255 9592 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 19111586
5311111 8956 0 None -1 2 Mouse 9.3 pIC50 = 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
650 8956 0 None -1 2 Mouse 9.3 pIC50 = 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
122227 8160 31 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3825 8160 31 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
644 8160 31 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL264100 8160 31 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
678 10580 0 None -5 2 Human 6.3 pIC50 None 6.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
119343 9649 22 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
676 9649 22 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL446325 9649 22 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
123973 9648 0 None -79 2 Human 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
675 9648 0 None -79 2 Human 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
678 10580 0 None 5 2 Mouse 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
673 8466 15 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
9810391 8466 15 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
CHEMBL1192627 8466 15 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
671 10669 0 None -1 2 Human 8.0 pIC50 None 8 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
671 10669 0 None 1 2 Mouse 8.1 pIC50 None 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3035449 9294 0 None -1 3 Mouse 8.4 pIC50 None 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
638 9294 0 None -1 3 Mouse 8.4 pIC50 None 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3035449 9294 0 None 1 3 Human 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
638 9294 0 None 1 3 Human 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
119343 9649 22 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
676 9649 22 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL446325 9649 22 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
123973 9648 0 None 79 2 Mouse 8.9 pIC50 None 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
675 9648 0 None 79 2 Mouse 8.9 pIC50 None 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
10394861 8470 5 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
669 8470 5 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
CHEMBL329762 8470 5 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
3812 7504 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
439201 7504 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
649 7504 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL406291 7504 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB12126 7504 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
5311111 8956 0 None 1 2 Human 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
650 8956 0 None 1 2 Human 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267




Ligands Receptor Assay information Chemical information
Sel. page Common
name
GPCRdb ID #Vendors Reference
ligand
Fold selectivity
(Affinity)
# tested GPCRs
(Affinity)
Species p-value
(-log)
Type Activity
Relation
Activity
Value
Assay Type Assay Description Source Mol
weight
Rot
Bonds
H don H acc LogP Smiles DOI
11980903 21264 19 None - 0 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 382 4 0 2 5.3 Cc1cc(/C=C/c2ccc3cc(N(C)C)ccc3[n+]2C)c(C)n1-c1ccccc1 10.1038/s41467-023-40064-9
22526 21264 19 None - 0 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 382 4 0 2 5.3 Cc1cc(/C=C/c2ccc3cc(N(C)C)ccc3[n+]2C)c(C)n1-c1ccccc1 10.1038/s41467-023-40064-9
5281035 21264 19 None - 0 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 382 4 0 2 5.3 Cc1cc(/C=C/c2ccc3cc(N(C)C)ccc3[n+]2C)c(C)n1-c1ccccc1 10.1038/s41467-023-40064-9
CHEMBL1201303 21264 19 None - 0 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 382 4 0 2 5.3 Cc1cc(/C=C/c2ccc3cc(N(C)C)ccc3[n+]2C)c(C)n1-c1ccccc1 10.1038/s41467-023-40064-9
137 7158 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
2119 7158 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
563 7158 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
66368 7158 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
CHEMBL266195 7158 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
DB00866 7158 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
6436173 61890 45 None - 0 Human 4.8 pAC50 = 4.8 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 785 2 5 13 6.2 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c5c(nc6cc(C)ccn65)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
CHEMBL1617 61890 45 None - 0 Human 4.8 pAC50 = 4.8 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 785 2 5 13 6.2 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c5c(nc6cc(C)ccn65)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
135398735 143746 32 None - 0 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 822 4 6 15 4.3 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
136262914 143746 32 None - 0 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 822 4 6 15 4.3 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
CHEMBL374478 143746 32 None - 0 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 822 4 6 15 4.3 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
4495 203314 92 None - 29 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 308 5 1 5 2.8 CS(=O)(=O)Nc1ccc([N+](=O)[O-])cc1Oc1ccccc1 10.1038/s41467-023-40064-9
CHEMBL56367 203314 92 None - 29 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 308 5 1 5 2.8 CS(=O)(=O)Nc1ccc([N+](=O)[O-])cc1Oc1ccccc1 10.1038/s41467-023-40064-9
5329102 201505 86 None - 0 Human 5.6 pAC50 = 5.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 398 7 3 3 3.3 CCN(CC)CCNC(=O)c1c(C)[nH]c(/C=C2\C(=O)Nc3ccc(F)cc32)c1C 10.1038/s41467-023-40064-9
CHEMBL535 201505 86 None - 0 Human 5.6 pAC50 = 5.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 398 7 3 3 3.3 CCN(CC)CCNC(=O)c1c(C)[nH]c(/C=C2\C(=O)Nc3ccc(F)cc32)c1C 10.1038/s41467-023-40064-9
135564886 21265 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
135673376 21265 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
137157436 21265 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
145948239 21265 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
71587099 21265 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
CHEMBL1201304 21265 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
26248 168318 102 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 368 3 1 7 2.0 CC(=O)Oc1cccc2c1C(=O)c1c(OC(C)=O)cc(C(=O)O)cc1C2=O 10.1038/s41467-023-40064-9
CHEMBL41286 168318 102 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 368 3 1 7 2.0 CC(=O)Oc1cccc2c1C(=O)c1c(OC(C)=O)cc(C(=O)O)cc1C2=O 10.1038/s41467-023-40064-9
2335 18620 22 None - 12 Human 4.5 pAC50 = 4.5 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 412 11 0 2 6.1 CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1 10.1038/s41467-023-40064-9
8478 18620 22 None - 12 Human 4.5 pAC50 = 4.5 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 412 11 0 2 6.1 CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1 10.1038/s41467-023-40064-9
CHEMBL1182210 18620 22 None - 12 Human 4.5 pAC50 = 4.5 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 412 11 0 2 6.1 CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1 10.1038/s41467-023-40064-9
CHEMBL221753 18620 22 None - 12 Human 4.5 pAC50 = 4.5 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 412 11 0 2 6.1 CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1 10.1038/s41467-023-40064-9
41684 37995 105 None - 0 Human 5.3 pAC50 = 5.3 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 307 4 1 7 2.2 CC(=O)Oc1ccccc1C(=O)Nc1ncc([N+](=O)[O-])s1 10.1038/s41467-023-40064-9
CHEMBL1401 37995 105 None - 0 Human 5.3 pAC50 = 5.3 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 307 4 1 7 2.2 CC(=O)Oc1ccccc1C(=O)Nc1ncc([N+](=O)[O-])s1 10.1038/s41467-023-40064-9
2179 174297 76 None - 0 Human 5.1 pAC50 = 5.1 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 393 5 2 5 4.5 COc1cc(NS(C)(=O)=O)ccc1Nc1c2ccccc2nc2ccccc12 10.1038/s41467-023-40064-9
CHEMBL1256655 174297 76 None - 0 Human 5.1 pAC50 = 5.1 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 393 5 2 5 4.5 COc1cc(NS(C)(=O)=O)ccc1Nc1c2ccccc2nc2ccccc12 10.1038/s41467-023-40064-9
CHEMBL43 174297 76 None - 0 Human 5.1 pAC50 = 5.1 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 393 5 2 5 4.5 COc1cc(NS(C)(=O)=O)ccc1Nc1c2ccccc2nc2ccccc12 10.1038/s41467-023-40064-9
11498853 89963 13 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL218427 89963 13 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL541758 89963 13 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
667 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
6918173 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
667 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
6918173 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
71364 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
CHEMBL2028850 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
DB06196 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
667 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
6918173 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
71364 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2028850 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
DB06196 8754 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2370160 216581 0 None - 0 Guinea pig 10.1 pIC50 = 10.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CS)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1c2ccccc2C[C@@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm030326t
11801968 20483 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194974 20483 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553614 20483 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
11250851 20389 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1194270 20389 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3216880 20389 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
9874617 20078 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191908 20078 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543070 20078 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11250929 20607 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1195824 20607 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL555403 20607 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
11158089 19689 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189084 19689 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538022 19689 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
18704946 19942 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1190879 19942 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3217081 19942 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
44214214 20033 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191492 20033 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL542598 20033 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
44360533 19664 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1188925 19664 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL537683 19664 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10009762 19701 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
CHEMBL1189175 19701 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
CHEMBL3217072 19701 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
10009762 19701 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1189175 19701 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217072 19701 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10627384 20510 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL1195129 20510 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL553911 20510 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
11490839 19941 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190878 19941 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL541805 19941 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11273808 20570 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195573 20570 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3215979 20570 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
22008895 117335 0 None - 1 Guinea pig 9.5 pIC50 = 9.5 Binding
Displacement of [3H]bradykinin from guinea pig B2 receptorDisplacement of [3H]bradykinin from guinea pig B2 receptor
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1021/jm9002445
CHEMBL325255 117335 0 None - 1 Guinea pig 9.5 pIC50 = 9.5 Binding
Displacement of [3H]bradykinin from guinea pig B2 receptorDisplacement of [3H]bradykinin from guinea pig B2 receptor
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1021/jm9002445
11445288 20648 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1196072 20648 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217085 20648 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11262728 145242 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1016/j.ejmech.2020.112948
CHEMBL3774617 145242 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1016/j.ejmech.2020.112948
11802489 20505 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1195106 20505 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL553844 20505 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11262728 145242 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/acs.jmedchem.5b00982
CHEMBL3774617 145242 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/acs.jmedchem.5b00982
44329173 174591 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 787 14 2 9 7.4 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL430652 174591 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 787 14 2 9 7.4 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
44360597 20656 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL1196121 20656 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL555976 20656 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
10349737 19888 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1190430 19888 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL540840 19888 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11411675 103270 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL262507 103270 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
5311114 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
668 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
CHEMBL99869 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
5311114 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
668 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
CHEMBL99869 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
5311114 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
668 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
CHEMBL99869 8469 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
44360533 19664 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1188925 19664 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL537683 19664 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
44360877 20459 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1194797 20459 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL553315 20459 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
11491041 20228 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1193122 20228 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL544480 20228 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11227974 20077 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191906 20077 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543068 20077 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
10652092 19789 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189828 19789 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL539550 19789 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
5311108 8467 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
674 8467 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
CHEMBL130517 8467 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
10531497 19985 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
CHEMBL1191172 19985 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
CHEMBL542232 19985 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
5311108 8467 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
674 8467 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
CHEMBL130517 8467 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
10674687 20399 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1194363 20399 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL552543 20399 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
11251046 19977 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191121 19977 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542173 19977 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
667 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
6918173 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
71364 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2028850 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
DB06196 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2370160 216581 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CS)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1c2ccccc2C[C@@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm030326t
667 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
6918173 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 8754 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
11802476 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
10698671 20240 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1193229 20240 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL544599 20240 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11802476 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189415 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538732 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
11802476 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1189415 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL538732 19736 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10348414 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL439737 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL542096 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10348414 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL439737 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL542096 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL439737 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL542096 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL439737 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL542096 175852 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
44360968 127862 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL357075 127862 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
10371910 26906 1 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130436 26906 1 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
11411594 19680 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189023 19680 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL537927 19680 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
44360818 20250 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL1193250 20250 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL544623 20250 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
10555818 20457 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194778 20457 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553293 20457 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
10675847 20189 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1192831 20189 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL544134 20189 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44361029 20138 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1192448 20138 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL543685 20138 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
11479739 214982 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98460 214982 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
44360597 20656 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL1196121 20656 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL555976 20656 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
44360877 20459 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1194797 20459 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL553315 20459 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
10604613 19885 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1190420 19885 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL540828 19885 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10580156 19883 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1190412 19883 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL540819 19883 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
11239595 20495 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195041 20495 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553762 20495 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10627384 20510 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL1195129 20510 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL553911 20510 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10675243 103555 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL264751 103555 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
10675243 103555 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
CHEMBL264751 103555 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
673 8466 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 8466 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 8466 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
673 8466 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
9810391 8466 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
CHEMBL1192627 8466 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
45269613 201633 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 695 12 3 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@H]4C(=O)CCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL539924 201633 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 695 12 3 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@H]4C(=O)CCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm9002445
10531497 19985 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL1191172 19985 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL542232 19985 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
10394861 8470 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
669 8470 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
CHEMBL329762 8470 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
44360879 19743 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1189464 19743 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL538784 19743 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10394861 8470 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
669 8470 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
CHEMBL329762 8470 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
9958759 20243 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1193231 20243 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL544601 20243 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
11445540 174952 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 727 13 2 8 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030468n
CHEMBL433214 174952 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 727 13 2 8 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030468n
10032884 20237 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193185 20237 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL544549 20237 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10257108 16603 1 None - 1 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 16603 1 None - 1 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
10371910 26906 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130436 26906 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10651980 20190 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192832 20190 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544135 20190 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
11365972 20415 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1194477 20415 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216391 20415 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
44360968 127862 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL357075 127862 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
44353012 20161 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192626 20161 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL543898 20161 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10721082 20067 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1191809 20067 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL542958 20067 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
10818426 20133 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192425 20133 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543657 20133 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10746610 20188 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192829 20188 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL544132 20188 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10578612 20504 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1195105 20504 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL553843 20504 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10722424 177738 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL44557 177738 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
10722424 177738 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL44557 177738 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
11491055 214980 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 723 12 1 7 7.3 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98459 214980 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 723 12 1 7 7.3 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030468n
44360553 20578 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1195619 20578 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL555006 20578 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
11377448 19827 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190058 19827 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216622 19827 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10842202 20618 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1195903 20618 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL555555 20618 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
9831859 16478 0 None - 1 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 16478 0 None - 1 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
11422541 214946 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL98292 214946 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10627732 29239 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL132510 29239 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
10769383 29637 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL132860 29637 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
10745254 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL143697 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL543781 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
10745254 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL143697 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL543781 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
10745254 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL143697 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL543781 42101 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10579332 20526 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 20526 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 20526 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10579332 20526 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195281 20526 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL554206 20526 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11239019 20259 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL1193332 20259 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL544720 20259 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
11468276 20285 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193590 20285 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL545021 20285 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10651897 19773 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1189702 19773 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL539294 19773 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
10841531 27330 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130782 27330 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
11801800 27932 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL131263 27932 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
10699672 19729 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189342 19729 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538531 19729 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10348414 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
CHEMBL439737 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
CHEMBL542096 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
10348414 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL439737 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL542096 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL439737 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL542096 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11456652 19979 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1191124 19979 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL542176 19979 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
11468051 20462 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1194820 20462 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215558 20462 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL439737 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL542096 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL439737 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL542096 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10348414 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 175852 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11216111 20062 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1191769 20062 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL542911 20062 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
11169915 20311 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1193789 20311 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL545255 20311 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11169975 214979 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL98458 214979 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
11169975 214979 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL98458 214979 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
11445066 20183 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1192789 20183 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL544087 20183 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
11456756 20581 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195624 20581 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216405 20581 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
22008895 117335 0 None - 1 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 117335 0 None - 1 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10603710 20433 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194615 20433 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL552986 20433 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
10348414 175852 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 175852 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 175852 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10603710 20433 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1194615 20433 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL552986 20433 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
44360617 20249 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1193249 20249 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL544622 20249 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10555195 20016 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1191388 20016 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL542479 20016 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
673 8466 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 8466 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 8466 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
11801941 20619 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1195904 20619 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL555556 20619 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10698666 20779 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1197062 20779 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL559195 20779 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10627456 26922 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130452 26922 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
673 8466 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
9810391 8466 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
CHEMBL1192627 8466 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
5311108 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
674 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
CHEMBL130517 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
11204833 118410 1 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 711 12 1 7 6.9 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL328509 118410 1 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 711 12 1 7 6.9 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030468n
11433973 119172 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL329701 119172 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
5311108 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
674 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
CHEMBL130517 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
5311108 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
674 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
CHEMBL130517 8467 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
11802476 19736 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 19736 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 19736 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
11802476 19736 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189415 19736 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538732 19736 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44360553 20578 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1195619 20578 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL555006 20578 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10721752 175997 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL44087 175997 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
10675847 20189 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1192831 20189 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL544134 20189 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10721752 175997 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL44087 175997 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
11308648 19807 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189935 19807 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539792 19807 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11445066 20183 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1192789 20183 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL544087 20183 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
122189857 130192 0 None - 2 Guinea pig 8.8 pIC50 = 8.8 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1742 42 23 22 -4.6 C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616881 130192 0 None - 2 Guinea pig 8.8 pIC50 = 8.8 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1742 42 23 22 -4.6 C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
122189855 130190 0 None - 3 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616879 130190 0 None - 3 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
3812 7504 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
439201 7504 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
649 7504 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
CHEMBL406291 7504 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
DB12126 7504 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
11399463 20229 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1193123 20229 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3143949 20229 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11399463 20229 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1193123 20229 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3143949 20229 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11445445 20490 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195018 20490 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3215999 20490 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
11204664 118350 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL328131 118350 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10651897 19773 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1189702 19773 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL539294 19773 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
122189856 130191 0 None - 1 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1858 43 22 22 -2.5 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616880 130191 0 None - 1 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1858 43 22 22 -2.5 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)O 10.1016/j.bmcl.2015.08.014
10531744 123121 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL335946 123121 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
10698671 20240 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1193229 20240 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL544599 20240 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
119343 9649 22 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
676 9649 22 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
CHEMBL446325 9649 22 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
45272156 201838 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL549534 201838 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190263 202733 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
CHEMBL559565 202733 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
18941145 16735 0 None - 1 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 16735 0 None - 1 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
10627129 108323 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL298320 108323 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
10627129 108323 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL298320 108323 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
10663541 126300 1 None - 0 Guinea pig 5.0 pIC50 = 5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 320 4 0 3 4.8 CCc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
CHEMBL345670 126300 1 None - 0 Guinea pig 5.0 pIC50 = 5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 320 4 0 3 4.8 CCc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
10818058 123362 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL336574 123362 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
10579547 20348 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194034 20348 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545534 20348 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10556247 29800 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL133005 29800 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
44341039 16283 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 16283 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
22008892 116939 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL323693 116939 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
10651074 108338 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 108338 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44189789 202932 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561223 202932 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190166 203413 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564294 203413 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10651074 108338 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL298463 108338 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10626618 40249 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
CHEMBL142015 40249 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
10603982 86860 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL21311 86860 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
10603982 86860 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL21311 86860 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10579143 175243 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL43510 175243 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10579143 175243 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 175243 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
18941161 16501 0 None - 1 Guinea pig 5.0 pIC50 = 5.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 16501 0 None - 1 Guinea pig 5.0 pIC50 = 5.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10675163 20014 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1191383 20014 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL542472 20014 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44190854 202224 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL552384 202224 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
19603349 19980 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191125 19980 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542177 19980 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
11296863 20182 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1192787 20182 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3216859 20182 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44353012 20161 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192626 20161 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL543898 20161 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10854681 126799 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 339 3 1 3 5.2 Cc1nc2c(NCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
CHEMBL350232 126799 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 339 3 1 3 5.2 Cc1nc2c(NCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
176 7186 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2157 7186 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2566 7186 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
CHEMBL633 7186 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
DB01118 7186 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
11169915 20311 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1193789 20311 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL545255 20311 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11445445 20490 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195018 20490 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3215999 20490 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
11801083 122026 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL334753 122026 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
10530740 172371 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL424268 172371 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
44189792 201914 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550142 201914 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44340818 117386 0 None - 1 Guinea pig 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 117386 0 None - 1 Guinea pig 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
11801800 27932 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL131263 27932 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
119343 9649 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
676 9649 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
CHEMBL446325 9649 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
44190941 202210 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
CHEMBL552296 202210 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
119343 9649 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
676 9649 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
CHEMBL446325 9649 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
11800992 125560 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL342016 125560 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10627732 29239 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL132510 29239 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
18941160 16687 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 16687 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10651302 20089 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192012 20089 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543188 20089 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
44190943 202732 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
CHEMBL559564 202732 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
10743094 52078 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 471 4 0 5 5.5 COC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL152650 52078 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 471 4 0 5 5.5 COC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL2392354 217194 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None N=C(N)NCCC[C@H](N)C(=O)N[C@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1016/j.ejmech.2013.01.044
10818067 20134 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1192427 20134 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL543659 20134 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10722378 28112 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 7 3 6 5.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131404 28112 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 7 3 6 5.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10698666 20779 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1197062 20779 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL559195 20779 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10651301 123306 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336209 123306 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10604425 171926 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL422794 171926 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10552342 54342 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCN(C(C)=O)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154625 54342 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCN(C(C)=O)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10744917 125614 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL342195 125614 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10503130 19776 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL1189725 19776 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL539324 19776 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
10737855 52773 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 368 3 0 3 4.8 Cc1nc2c(OCc3c(F)cccc3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL153271 52773 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 368 3 0 3 4.8 Cc1nc2c(OCc3c(F)cccc3Cl)cccn2c1Br 10.1021/jm970591c
11239381 19916 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1190638 19916 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215541 19916 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10601892 53805 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL154188 53805 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL558018 53805 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10699672 19729 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189342 19729 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538531 19729 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10601892 53805 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154188 53805 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL558018 53805 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10531338 98482 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL240875 98482 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
10531338 98482 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL240875 98482 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
10506334 126417 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 0 5 4.7 CC(=O)N(C)CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL346718 126417 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 0 5 4.7 CC(=O)N(C)CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11491041 20228 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1193122 20228 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL544480 20228 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11800992 125560 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL342016 125560 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10744917 125614 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL342195 125614 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10579159 126085 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
CHEMBL344021 126085 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
10674242 30929 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL133913 30929 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
11801594 107208 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 107208 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
11801594 107208 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL290431 107208 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
10693943 126388 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 428 3 0 3 5.4 Cc1nc2c(OCc3c(Br)cccc3Br)cccn2c1Cl 10.1021/jm970591c
CHEMBL346458 126388 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 428 3 0 3 5.4 Cc1nc2c(OCc3c(Br)cccc3Br)cccn2c1Cl 10.1021/jm970591c
10554743 121932 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL334421 121932 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
44190752 202125 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
CHEMBL551759 202125 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
10508305 20381 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194233 20381 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545765 20381 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10836951 54264 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 4 1 4 5.2 CC(=O)Nc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154558 54264 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 4 1 4 5.2 CC(=O)Nc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10518915 126342 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 308 3 0 3 4.2 Cc1nc2c(OCc3c(F)cccc3F)cccn2c1Cl 10.1021/jm970591c
CHEMBL346034 126342 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 308 3 0 3 4.2 Cc1nc2c(OCc3c(F)cccc3F)cccn2c1Cl 10.1021/jm970591c
10649831 20141 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1192462 20141 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL543700 20141 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11262636 20609 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1195841 20609 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215972 20609 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11801941 20619 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1195904 20619 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL555556 20619 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10841637 20691 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1196403 20691 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL556816 20691 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
11181406 19710 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL1189212 19710 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL3217073 19710 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
11479285 19927 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190741 19927 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3143958 19927 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11479285 19927 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190741 19927 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3143958 19927 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10650330 19932 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1190789 19932 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL541590 19932 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10604425 171926 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL422794 171926 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10722424 177738 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL44557 177738 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
19603349 19980 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191125 19980 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542177 19980 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
673 8466 15 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 8466 15 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 8466 15 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
10722424 177738 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL44557 177738 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
5311114 8469 8 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
668 8469 8 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
CHEMBL99869 8469 8 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
10841582 20015 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1191384 20015 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL542473 20015 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
9894265 38312 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL140383 38312 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10793563 20612 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195858 20612 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL555465 20612 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10769517 30228 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL133339 30228 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
10840534 29345 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL132620 29345 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
10349737 19888 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1190430 19888 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL540840 19888 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
10840534 29345 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL132620 29345 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm970591c
11320262 214958 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 775 14 2 9 7.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)Cc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98349 214958 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 775 14 2 9 7.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)Cc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
11181524 214800 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
CHEMBL97393 214800 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
11193509 20509 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195125 20509 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553897 20509 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
10818067 20134 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1192427 20134 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL543659 20134 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10793563 20612 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195858 20612 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL555465 20612 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10842202 20618 1 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1195903 20618 1 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL555555 20618 1 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
11343115 19846 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1190165 19846 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL540300 19846 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
44360818 20250 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL1193250 20250 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL544623 20250 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
9894265 38312 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL140383 38312 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10651302 20089 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192012 20089 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543188 20089 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10604560 27177 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL130660 27177 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11250851 20389 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1194270 20389 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3216880 20389 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11296863 20182 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1192787 20182 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3216859 20182 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10769485 27322 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL130775 27322 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10746877 20590 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1195721 20590 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL555202 20590 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
11479285 19927 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190741 19927 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3143958 19927 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11479285 19927 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190741 19927 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3143958 19927 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
11343115 19846 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1190165 19846 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL540300 19846 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
10818426 20133 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192425 20133 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543657 20133 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10651980 20190 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192832 20190 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544135 20190 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190269 202975 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561415 202975 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10555263 107873 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295005 107873 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
10841582 20015 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1191384 20015 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL542473 20015 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
44191220 201809 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL549337 201809 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190168 201897 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550016 201897 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191224 203040 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561839 203040 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10569271 56760 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 340 3 0 3 5.2 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
CHEMBL156902 56760 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 340 3 0 3 5.2 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
10555263 107873 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295005 107873 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
10699094 30033 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 30033 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
127034153 145342 0 None - 0 Human 4.7 pIC50 = 4.7 Binding
Inhibition of recombinant human bradykinin receptor 2 expressed in CHO cellsInhibition of recombinant human bradykinin receptor 2 expressed in CHO cells
ChEMBL 365 5 2 3 4.5 CC(C)CN1[C@H](C)Cc2cc(O)ccc2[C@H]1c1ccc(/C=C/C(=O)O)cc1 10.1021/acsmedchemlett.5b00413
CHEMBL3775378 145342 0 None - 0 Human 4.7 pIC50 = 4.7 Binding
Inhibition of recombinant human bradykinin receptor 2 expressed in CHO cellsInhibition of recombinant human bradykinin receptor 2 expressed in CHO cells
ChEMBL 365 5 2 3 4.5 CC(C)CN1[C@H](C)Cc2cc(O)ccc2[C@H]1c1ccc(/C=C/C(=O)O)cc1 10.1021/acsmedchemlett.5b00413
1016 10519 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2561 10519 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2733526 10519 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
5384 10519 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
CHEMBL83 10519 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
DB00675 10519 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
72548703 168346 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysisDisplacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysis
ChEMBL 583 8 3 6 5.8 CC(C)(C)NS(=O)(=O)c1ccc(-c2sc(C(=O)N[C@H]3C[C@H](C(=O)O)C3)nc2CC2CCCCC2)c2ccccc12 10.1016/j.bmcl.2018.03.093
CHEMBL4128926 168346 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysisDisplacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysis
ChEMBL 583 8 3 6 5.8 CC(C)(C)NS(=O)(=O)c1ccc(-c2sc(C(=O)N[C@H]3C[C@H](C(=O)O)C3)nc2CC2CCCCC2)c2ccccc12 10.1016/j.bmcl.2018.03.093
11296704 20597 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL1195759 20597 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL3216408 20597 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
22008929 16522 0 None - 1 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 16522 0 None - 1 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190268 203290 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563516 203290 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10579159 126085 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
CHEMBL344021 126085 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
10791325 51536 0 None - 0 Guinea pig 5.7 pIC50 = 5.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 491 5 0 5 4.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)S(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL152158 51536 0 None - 0 Guinea pig 5.7 pIC50 = 5.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 491 5 0 5 4.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)S(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
10841393 20055 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL1191700 20055 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL542836 20055 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
10841393 20055 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL1191700 20055 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL542836 20055 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
10792967 85302 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL2111974 85302 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10507708 168602 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL41446 168602 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
10507708 168602 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL41446 168602 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
9851817 16453 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 16453 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
10762703 54029 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 384 3 0 3 5.3 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL154386 54029 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 384 3 0 3 5.3 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Br 10.1021/jm970591c
44323787 19788 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189812 19788 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215529 19788 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11468071 19809 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189943 19809 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL539800 19809 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10555061 123744 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL338682 123744 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11411594 19680 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189023 19680 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL537927 19680 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11239502 20475 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1194911 20475 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL553530 20475 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
44340760 117285 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 117285 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
11468071 19809 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189943 19809 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL539800 19809 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11181524 214800 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
CHEMBL97393 214800 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
10816636 20539 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1195365 20539 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL554412 20539 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10841531 27330 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130782 27330 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
44214279 16488 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 16488 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
10675163 20014 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1191383 20014 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL542472 20014 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10507708 168602 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL41446 168602 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
10507708 168602 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL41446 168602 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
11422667 19757 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189575 19757 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539023 19757 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11456756 20581 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195624 20581 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216405 20581 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
10555202 123530 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
CHEMBL337555 123530 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
11468276 20285 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193590 20285 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL545021 20285 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
15388873 121509 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL333832 121509 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
11801594 107208 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL290431 107208 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
11801594 107208 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 107208 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
10009762 19701 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1189175 19701 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217072 19701 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10579332 20526 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 20526 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 20526 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11239019 20259 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL1193332 20259 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL544720 20259 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
11399463 20229 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1193123 20229 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3143949 20229 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11399463 20229 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1193123 20229 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3143949 20229 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44361029 20138 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1192448 20138 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL543685 20138 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
10555818 20457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194778 20457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553293 20457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
10746877 20590 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1195721 20590 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL555202 20590 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
667 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
6918173 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
667 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
6918173 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
71364 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
CHEMBL2028850 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
DB06196 8754 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
9874617 20078 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191908 20078 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543070 20078 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10674242 30929 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL133913 30929 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
11169752 119186 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL329758 119186 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10652092 19789 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189828 19789 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL539550 19789 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11273808 20570 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195573 20570 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3215979 20570 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11491069 19688 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189082 19688 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538020 19688 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10841637 20691 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1196403 20691 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL556816 20691 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10580536 19712 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189218 19712 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL538281 19712 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10603710 20433 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1194615 20433 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL552986 20433 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
44360617 20249 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1193249 20249 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL544622 20249 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10603710 20433 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194615 20433 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL552986 20433 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
11491069 19688 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189082 19688 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538020 19688 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11365972 20415 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1194477 20415 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216391 20415 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10818058 123362 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL336574 123362 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
10840241 123247 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336116 123247 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
44191226 202081 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551435 202081 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10756101 52855 4 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 292 3 0 3 4.2 Clc1cccc(Cl)c1COc1cccn2ccnc12 10.1021/jm970591c
CHEMBL153344 52855 4 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 292 3 0 3 4.2 Clc1cccc(Cl)c1COc1cccn2ccnc12 10.1021/jm970591c
44369201 128235 0 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 381 5 0 4 5.8 CCn1c(C)cc(C#N)c1-c1ccc(COc2cc(C)nc3ccccc23)cc1 10.1021/jm970591c
CHEMBL358232 128235 0 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 381 5 0 4 5.8 CCn1c(C)cc(C#N)c1-c1ccc(COc2cc(C)nc3ccccc23)cc1 10.1021/jm970591c
44191225 203175 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562747 203175 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2372276 216985 0 None 3 3 Human 7.5 pIC50 = 7.5 Binding
Displacement of radiolabeled NPC 567 from human bradykinin B2 receptorDisplacement of radiolabeled NPC 567 from human bradykinin B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm8007618
44341214 117207 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 117207 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190853 203068 4 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
CHEMBL562097 203068 4 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
11250929 20607 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
CHEMBL1195824 20607 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
CHEMBL555403 20607 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
11250929 20607 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1195824 20607 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL555403 20607 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
10579723 28089 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131380 28089 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
9958759 20243 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1193231 20243 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL544601 20243 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
10699094 30033 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 30033 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
10627456 26922 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130452 26922 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10504612 127908 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 4 1 4 5.1 CNC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL357530 127908 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 4 1 4 5.1 CNC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10699094 30033 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 30033 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
44190756 202216 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552359 202216 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
44189790 203421 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564341 203421 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190754 203227 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563068 203227 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
11239595 20495 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195041 20495 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553762 20495 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11433935 19978 1 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191123 19978 1 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215986 19978 1 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10531338 98482 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL240875 98482 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
10531338 98482 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL240875 98482 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
10579143 175243 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 175243 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10790603 51938 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 5 1 5 4.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CN)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL152542 51938 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 5 1 5 4.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CN)c3Cl)cccn2c1Br 10.1021/jm970591c
10579143 175243 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL43510 175243 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10555195 20016 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1191388 20016 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL542479 20016 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
44346506 18211 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
CHEMBL1180320 18211 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
CHEMBL121851 18211 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
44340964 16479 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 16479 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190944 202712 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559436 202712 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
11479294 20596 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195758 20596 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216404 20596 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
11801083 122026 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL334753 122026 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
10604613 19885 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1190420 19885 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL540828 19885 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11422541 214946 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL98292 214946 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10508305 20381 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194233 20381 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545765 20381 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
18923274 26597 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130196 26597 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10675243 103555 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
CHEMBL264751 103555 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
11490605 20523 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1195242 20523 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL554127 20523 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10675243 103555 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL264751 103555 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
11445288 20648 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1196072 20648 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217085 20648 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
18704946 19942 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1190879 19942 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3217081 19942 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11169752 119186 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL329758 119186 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
44360879 19743 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1189464 19743 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL538784 19743 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10531497 19985 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL1191172 19985 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL542232 19985 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
10580536 19712 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189218 19712 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL538281 19712 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10745254 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL143697 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL543781 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
11296704 20597 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL1195759 20597 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL3216408 20597 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
10745254 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL143697 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL543781 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10745254 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL143697 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL543781 42101 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
11193509 20509 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195125 20509 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553897 20509 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11331301 20059 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191763 20059 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215537 20059 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44375675 63280 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
In vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assayIn vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assay
ChEMBL 605 12 4 7 4.9 O=C(O)CN(Cc1ccccc1)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1016/s0960-894x(01)00044-0
CHEMBL163506 63280 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
In vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assayIn vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assay
ChEMBL 605 12 4 7 4.9 O=C(O)CN(Cc1ccccc1)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1016/s0960-894x(01)00044-0
10789357 54347 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 5 0 4 5.7 CCN(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154633 54347 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 5 0 4 5.7 CCN(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10601892 53805 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL154188 53805 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL558018 53805 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11796916 56754 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 429 4 0 5 5.2 Cc1nc2c(OCc3c(Cl)ccc([N+](=O)[O-])c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL156899 56754 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 429 4 0 5 5.2 Cc1nc2c(OCc3c(Cl)ccc([N+](=O)[O-])c3Cl)cccn2c1Br 10.1021/jm970591c
44190165 202742 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559645 202742 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11799290 56699 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 489 4 0 4 5.9 CC(=O)N(C)c1c(Cl)cc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL156847 56699 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 489 4 0 4 5.9 CC(=O)N(C)c1c(Cl)cc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10555202 123530 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
CHEMBL337555 123530 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
9916589 107014 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 107014 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
11377448 19827 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190058 19827 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216622 19827 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
44190361 201582 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL538865 201582 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11801594 107208 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 107208 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
10531744 123121 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL335946 123121 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
44191221 203016 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2cncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561701 203016 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2cncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10852230 56391 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 306 3 0 3 4.5 Cc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
CHEMBL156606 56391 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 306 3 0 3 4.5 Cc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
10792291 20667 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1196218 20667 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL556176 20667 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10769517 30228 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL133339 30228 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
44214619 117382 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 117382 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
44190751 202124 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from wild-type B2 receptorDisplacement of [3H]bradykinin from wild-type B2 receptor
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 202124 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from wild-type B2 receptorDisplacement of [3H]bradykinin from wild-type B2 receptor
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
10721082 20067 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1191809 20067 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL542958 20067 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
10530740 172371 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL424268 172371 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
10675204 175559 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
CHEMBL43746 175559 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
10675204 175559 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
CHEMBL43746 175559 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
10603884 26909 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130438 26909 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11331301 20059 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191763 20059 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215537 20059 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11796407 54549 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 418 3 0 3 5.9 Cc1nc2c(OCc3c(Cl)ccc(Cl)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL154823 54549 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 418 3 0 3 5.9 Cc1nc2c(OCc3c(Cl)ccc(Cl)c3Cl)cccn2c1Br 10.1021/jm970591c
44190942 203006 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
CHEMBL561634 203006 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
10032884 20237 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193185 20237 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL544549 20237 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10626618 40249 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
CHEMBL142015 40249 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
10579332 20526 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195281 20526 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL554206 20526 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
44340859 16815 0 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 16815 0 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
11801968 20483 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194974 20483 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553614 20483 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
10579332 20526 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 20526 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 20526 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10793528 20242 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1193230 20242 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544600 20242 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190581 202723 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL559506 202723 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
10555061 123744 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL338682 123744 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11181406 19710 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL1189212 19710 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL3217073 19710 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
10769485 27322 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL130775 27322 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
11422667 19757 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189575 19757 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539023 19757 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11158136 215223 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 664 12 3 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)O)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL99978 215223 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 664 12 3 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)O)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
44190751 202124 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 202124 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
44189787 203123 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562434 203123 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10553878 54404 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 513 6 0 6 4.8 CC(=O)OCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154682 54404 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 513 6 0 6 4.8 CC(=O)OCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10842026 103497 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 655 10 2 6 6.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(-c3ccccc3)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL264259 103497 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 655 10 2 6 6.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(-c3ccccc3)n4C)c2Cl)cc1 10.1021/jm980300f
18923274 26597 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130196 26597 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10579723 28089 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131380 28089 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190672 202123 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551757 202123 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
10722735 26836 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130379 26836 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
22008916 16534 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 16534 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44190363 202082 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 318 3 0 3 4.8 Cc1ccc2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551436 202082 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 318 3 0 3 4.8 Cc1ccc2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10575810 128256 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 455 4 0 4 5.3 CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL358234 128256 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 455 4 0 4 5.3 CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10693220 54141 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 414 4 0 4 5.3 COc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154465 54141 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 414 4 0 4 5.3 COc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651074 108338 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL298463 108338 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10651074 108338 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 108338 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44340951 16774 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 16774 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
11262636 20609 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1195841 20609 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215972 20609 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10579547 20348 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194034 20348 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545534 20348 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10650330 19932 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1190789 19932 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL541590 19932 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
44191138 202695 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559273 202695 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10578574 20355 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL1194067 20355 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL545573 20355 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
10743570 53718 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 485 6 0 5 4.9 COCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154122 53718 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 485 6 0 5 4.9 COCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651074 108338 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 108338 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10554743 121932 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL334421 121932 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
45267862 203099 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL562296 203099 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
11227974 20077 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191906 20077 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543068 20077 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
11479739 214982 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98460 214982 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
10556247 29800 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL133005 29800 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
10394861 8470 5 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
669 8470 5 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
CHEMBL329762 8470 5 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
11490605 20523 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1195242 20523 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL554127 20523 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
44190755 202606 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL558279 202606 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190851 203349 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563878 203349 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
44214214 20033 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191492 20033 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL542598 20033 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11251046 19977 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191121 19977 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542173 19977 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
44190169 202067 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2ocnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551354 202067 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2ocnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10746610 20188 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192829 20188 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL544132 20188 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11239502 20475 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1194911 20475 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL553530 20475 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10506663 28204 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL131517 28204 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10722735 26836 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130379 26836 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190167 203268 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563391 203268 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10895913 16641 0 None - 1 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 16641 0 None - 1 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
11204664 118350 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL328131 118350 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
9916589 107014 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL288603 107014 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
9916589 107014 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 107014 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
10793528 20242 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1193230 20242 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544600 20242 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10793125 106953 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL288079 106953 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
10793125 106953 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL288079 106953 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
44190077 203249 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563254 203249 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11468051 20462 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1194820 20462 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215558 20462 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
119343 9649 22 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
676 9649 22 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
CHEMBL446325 9649 22 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
10721752 175997 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL44087 175997 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
10721752 175997 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL44087 175997 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
44190753 203482 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL564841 203482 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
10580156 19883 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1190412 19883 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL540819 19883 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
44190850 202002 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL550827 202002 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
10816618 20546 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1195382 20546 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL554431 20546 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10792967 85302 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL2111974 85302 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
44189791 203345 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2nncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563861 203345 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2nncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10672078 55058 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL155339 55058 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11801411 108121 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL296865 108121 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
11801411 108121 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL296865 108121 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
10604560 27177 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL130660 27177 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11308648 19807 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189935 19807 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539792 19807 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10568916 53442 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 336 4 1 4 4.0 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1CO 10.1021/jm970591c
CHEMBL153890 53442 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 336 4 1 4 4.0 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1CO 10.1021/jm970591c
13825921 51834 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 374 6 0 4 4.7 C#CCOCc1c(C)nc2c(OCc3c(Cl)cccc3Cl)cccn12 10.1021/jm970591c
CHEMBL152439 51834 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 374 6 0 4 4.7 C#CCOCc1c(C)nc2c(OCc3c(Cl)cccc3Cl)cccn12 10.1021/jm970591c
11216111 20062 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1191769 20062 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL542911 20062 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
15388870 117410 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL325742 117410 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
10768499 53727 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 1 5 4.8 CC(=O)NC(C)C(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154130 53727 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 1 5 4.8 CC(=O)NC(C)C(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10745895 107932 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295428 107932 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
10745895 107932 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295428 107932 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
11158089 19689 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189084 19689 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538022 19689 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11479294 20596 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195758 20596 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216404 20596 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
44190852 202185 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552090 202185 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
10578612 20504 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1195105 20504 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL553843 20504 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10769383 29637 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL132860 29637 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
10841393 20055 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL1191700 20055 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL542836 20055 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
25019714 203362 2 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL563956 203362 2 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
10841393 20055 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL1191700 20055 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL542836 20055 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
44191040 202763 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559825 202763 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
10675204 175559 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
CHEMBL43746 175559 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
10603884 26909 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130438 26909 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10506663 28204 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL131517 28204 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10506663 28204 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL131517 28204 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10675204 175559 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
CHEMBL43746 175559 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
44190267 201915 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550143 201915 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44341060 16332 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112360 16332 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10625996 127786 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CC(=O)NCCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL356480 127786 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CC(=O)NCCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651301 123306 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336209 123306 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10840534 29345 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL132620 29345 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
11433935 19978 1 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191123 19978 1 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215986 19978 1 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10603982 86860 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL21311 86860 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10603982 86860 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL21311 86860 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
11456652 19979 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1191124 19979 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL542176 19979 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10579143 175243 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 175243 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44323787 19788 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189812 19788 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215529 19788 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10840241 123247 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336116 123247 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10840241 123247 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL336116 123247 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11802476 19736 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1189415 19736 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL538732 19736 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
11802476 19736 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 19736 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 19736 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
9916589 107014 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 107014 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
11802489 20505 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1195106 20505 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL553844 20505 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11490839 19941 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190878 19941 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL541805 19941 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
9916589 107014 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL288603 107014 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
10674687 20399 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1194363 20399 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL552543 20399 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
10745895 107932 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295428 107932 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
10745895 107932 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295428 107932 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
11801411 108121 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL296865 108121 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
44191223 203046 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561899 203046 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11801411 108121 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL296865 108121 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10627129 108323 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL298320 108323 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
10627129 108323 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL298320 108323 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
10793125 106953 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL288079 106953 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
10793125 106953 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL288079 106953 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
10555263 107873 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295005 107873 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
10626599 37760 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 555 8 2 4 7.4 CNC(=O)c1ccc(/C=C/C(=O)Nc2cccc(-c3ccc(C)c(COc4cccc5ccc(C)nc45)c3C)c2)cc1 10.1021/jm980330i
CHEMBL139870 37760 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 555 8 2 4 7.4 CNC(=O)c1ccc(/C=C/C(=O)Nc2cccc(-c3ccc(C)c(COc4cccc5ccc(C)nc45)c3C)c2)cc1 10.1021/jm980330i
10555263 107873 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295005 107873 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
11239381 19916 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1190638 19916 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215541 19916 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44190266 202235 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL552442 202235 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL5274928 200610 0 None - 1 Human 9.4 pKd = 9.4 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1290 30 18 17 -4.8 N=C(N)NCCCC(NC(=O)[C@@H]1C[C@@H]2CCC[C@@H]2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
CHEMBL5280457 200847 0 None - 1 Human 9.1 pKd = 9.1 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1312 30 18 17 -4.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1Cc2ccccc2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
44317520 111666 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 601 12 5 5 3.6 N=C(N)NCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
CHEMBL311191 111666 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 601 12 5 5 3.6 N=C(N)NCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
44317577 212424 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 382 9 2 4 5.2 CCCCC1(CCCC)Oc2cccc(NC(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
CHEMBL81864 212424 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 382 9 2 4 5.2 CCCCC1(CCCC)Oc2cccc(NC(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
44317502 212512 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 439 12 2 5 5.0 CCCCC1(CCCC)Oc2cccc(N(CCCN)C(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
CHEMBL82600 212512 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 439 12 2 5 5.0 CCCCC1(CCCC)Oc2cccc(N(CCCN)C(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
44317490 111473 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 402 6 3 3 3.1 N=C(N)NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
CHEMBL310531 111473 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 402 6 3 3 3.1 N=C(N)NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
44317519 112516 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 531 11 2 5 5.1 NCCCN1C(=O)C(CCN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
CHEMBL312658 112516 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 531 11 2 5 5.1 NCCCN1C(=O)C(CCN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
44317631 111902 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 501 11 4 5 3.7 NCc1ccc(CNC(=O)[C@@H](CN)n2cccc2CNC(=O)C(c2ccccc2)C2CCCCC2)cc1 10.1016/s0960-894x(00)00482-0
CHEMBL311420 111902 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 501 11 4 5 3.7 NCc1ccc(CNC(=O)[C@@H](CN)n2cccc2CNC(=O)C(c2ccccc2)C2CCCCC2)cc1 10.1016/s0960-894x(00)00482-0
CHEMBL5268547 200349 0 None - 1 Human 5.7 pKd = 5.7 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1250 30 18 17 -5.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1CCC[C@@]12Cc1ccccc1CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C2=O 10.1021/acs.jmedchem.6b01029
73351522 96164 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 861 10 7 9 0.9 NCCCC[C@@H]1NC(=O)[C@H](c2ccccc2)NC(=O)[C@H](CNC(=O)Cc2ccccc2)NC(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H](CN)NC1=O 10.1016/s0960-894x(00)00482-0
CHEMBL2369879 96164 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 861 10 7 9 0.9 NCCCC[C@@H]1NC(=O)[C@H](c2ccccc2)NC(=O)[C@H](CNC(=O)Cc2ccccc2)NC(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H](CN)NC1=O 10.1016/s0960-894x(00)00482-0
90662959 113364 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 769 8 7 7 1.6 N=C(N)NCCC[C@@H]1NC(=O)N2C3CCCCC3C[C@H]2C(=O)N2Cc3ccccc3C[C@@H]2C(=O)NCC[C@@H](NC(=O)CCc2ccccc2)C(=O)CCNC1=O 10.1016/s0960-894x(00)00482-0
CHEMBL3142416 113364 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 769 8 7 7 1.6 N=C(N)NCCC[C@@H]1NC(=O)N2C3CCCCC3C[C@H]2C(=O)N2Cc3ccccc3C[C@@H]2C(=O)NCC[C@@H](NC(=O)CCc2ccccc2)C(=O)CCNC1=O 10.1016/s0960-894x(00)00482-0
44317544 212467 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 471 18 1 3 7.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN(CCCC)CCCC)c1 10.1016/s0960-894x(00)00482-0
CHEMBL82249 212467 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 471 18 1 3 7.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN(CCCC)CCCC)c1 10.1016/s0960-894x(00)00482-0
CHEMBL5266183 200251 0 None - 1 Human 5.6 pKd = 5.6 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1210 31 19 17 -6.4 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1Cc2ccccc2CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
CHEMBL5271423 200462 0 None - 1 Human 5.6 pKd = 5.6 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1312 30 18 17 -4.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
44317810 112407 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 537 14 4 5 4.6 NCCCC[C@H](C(=O)NCc1ccc(CN)cc1)n1cccc1C(=O)NC(Cc1ccccc1)c1ccccc1 10.1016/s0960-894x(00)00482-0
CHEMBL312374 112407 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 537 14 4 5 4.6 NCCCC[C@H](C(=O)NCc1ccc(CN)cc1)n1cccc1C(=O)NC(Cc1ccccc1)c1ccccc1 10.1016/s0960-894x(00)00482-0
CHEMBL5267275 200294 0 None - 1 Human 5.5 pKd = 5.5 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1250 30 18 17 -5.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1CCC[C@]12Cc1ccccc1CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C2=O 10.1021/acs.jmedchem.6b01029
90663066 113365 0 None - 1 Guinea pig 5.5 pKd = 5.5 Binding
Functional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assayFunctional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142595 113365 0 None - 1 Guinea pig 5.5 pKd = 5.5 Binding
Functional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assayFunctional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL5274916 200608 0 None - 1 Human 5.4 pKd = 5.4 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1405 31 20 19 -4.2 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@H]1CSSC[C@@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC1=O 10.1021/acs.jmedchem.6b01029
10481702 111182 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 517 10 2 5 4.8 NCCCN1C(=O)C(CN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
CHEMBL310300 111182 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 517 10 2 5 4.8 NCCCN1C(=O)C(CN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
10371624 112201 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 615 13 5 5 4.0 N=C(N)NCCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
CHEMBL311969 112201 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 615 13 5 5 4.0 N=C(N)NCCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
44317826 212054 0 None - 1 Human 5.3 pKd = 5.3 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 435 10 3 3 4.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN=C(N)N)cc2)c1 10.1016/s0960-894x(00)00482-0
CHEMBL79057 212054 0 None - 1 Human 5.3 pKd = 5.3 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 435 10 3 3 4.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN=C(N)N)cc2)c1 10.1016/s0960-894x(00)00482-0
44317458 211976 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 359 11 2 3 4.7 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN)c1 10.1016/s0960-894x(00)00482-0
CHEMBL78487 211976 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 359 11 2 3 4.7 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN)c1 10.1016/s0960-894x(00)00482-0
44317602 212456 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 360 5 1 3 3.6 NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
CHEMBL82194 212456 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 360 5 1 3 3.6 NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
44317543 112102 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 393 9 2 3 5.3 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN)cc2)c1 10.1016/s0960-894x(00)00482-0
CHEMBL311593 112102 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 393 9 2 3 5.3 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN)cc2)c1 10.1016/s0960-894x(00)00482-0
44317849 110679 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 434 7 1 3 5.6 NCc1cccc(Cn2ccc3c2C(=O)C(Cc2ccccc2)(Cc2ccccc2)CC3)c1 10.1016/s0960-894x(00)00482-0
CHEMBL309221 110679 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 434 7 1 3 5.6 NCc1cccc(Cn2ccc3c2C(=O)C(Cc2ccccc2)(Cc2ccccc2)CC3)c1 10.1016/s0960-894x(00)00482-0
11050762 74449 0 None 5248 2 Rat 10.6 pKi = 10.6 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907651 74449 0 None 5248 2 Rat 10.6 pKi = 10.6 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
667 8754 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
6918173 8754 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
71364 8754 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
CHEMBL2028850 8754 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
DB06196 8754 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
57398326 78419 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956864 78419 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963558 78419 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401774 78368 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956863 78368 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963184 78368 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391279 78369 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956876 78369 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963185 78369 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394782 78418 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956855 78418 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963557 78418 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57403503 78440 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956856 78440 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963651 78440 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 89963 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL218427 89963 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL541758 89963 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 89963 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218427 89963 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL541758 89963 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
11600324 148774 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL387452 148774 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105746 168709 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415366 168709 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
667 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
6918173 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
71364 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
CHEMBL2028850 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
DB06196 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
57399981 78349 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956858 78349 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963148 78349 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401778 78353 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956870 78353 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963152 78353 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57390466 78415 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956719 78415 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963540 78415 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
667 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
6918173 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
71364 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2028850 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06196 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
3812 7504 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
439201 7504 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
649 7504 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
CHEMBL406291 7504 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
DB12126 7504 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
44355428 175913 0 None - 1 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1200 31 15 18 -5.4 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL440257 175913 0 None - 1 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1200 31 15 18 -5.4 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
667 8754 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
6918173 8754 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
71364 8754 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2028850 8754 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06196 8754 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
57399228 78347 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956720 78347 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963146 78347 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398324 78360 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956862 78360 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963164 78360 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57345657 78367 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 78367 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 78367 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396534 78439 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956854 78439 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963650 78439 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105703 143258 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373607 143258 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
90662945 113363 0 None - 1 Human 10.1 pKi = 10.1 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1298 30 15 17 -5.2 NC(N)=NCCC[C@H](N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1c2ccccc2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm990961s
CHEMBL3142396 113363 0 None - 1 Human 10.1 pKi = 10.1 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1298 30 15 17 -5.2 NC(N)=NCCC[C@H](N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1c2ccccc2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm990961s
CHEMBL2371961 216937 0 None - 1 Guinea pig 10.1 pKi = 10.1 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00069a016
57401770 78358 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956853 78358 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963162 78358 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401772 78363 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956857 78363 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963175 78363 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396538 78364 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956861 78364 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963176 78364 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105734 91047 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221285 91047 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9831859 16478 0 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 16478 0 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10257108 16603 1 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 16603 1 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
3812 7504 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
439201 7504 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
649 7504 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL406291 7504 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
DB12126 7504 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL2371961 216937 0 None - 1 Guinea pig 10.0 pKi = 10.0 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00035a015
667 8754 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
6918173 8754 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
71364 8754 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
CHEMBL2028850 8754 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
DB06196 8754 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
57402746 78348 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956721 78348 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963147 78348 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57402744 78356 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956718 78356 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963160 78356 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57400986 78357 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956723 78357 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963161 78357 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105690 90409 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220478 90409 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102701 144216 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375354 144216 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44337475 14854 0 None - 1 Human 9.8 pKi = 9.8 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 329 5 0 4 1.4 CC(=O)CN1CN(CCc2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL109123 14854 0 None - 1 Human 9.8 pKi = 9.8 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 329 5 0 4 1.4 CC(=O)CN1CN(CCc2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
57401784 78414 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956875 78414 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963532 78414 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105751 90004 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL218636 90004 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL2369941 216516 0 None - 1 Guinea pig 9.8 pKi = 9.8 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None CCCC1C[C@H](C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N(C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccsc2)NC(=O)CNC(=O)[C@@H]2CC[C@H](O)N2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1 10.1021/jm00062a018
CHEMBL3038098 217710 0 None - 1 Human 9.8 pKi = 9.8 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)CC1CCCCC1 10.1021/jm950716i
CHEMBL5274928 200610 0 None - 1 Human 9.7 pKi = 9.7 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1290 30 18 17 -4.8 N=C(N)NCCCC(NC(=O)[C@@H]1C[C@@H]2CCC[C@@H]2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
667 8754 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
6918173 8754 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
71364 8754 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
CHEMBL2028850 8754 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
DB06196 8754 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
57394780 78417 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956852 78417 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963556 78417 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57392147 78444 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1955876 78444 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963660 78444 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105696 89983 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218540 89983 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441297 143666 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374224 143666 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
11766718 143711 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374272 143711 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9897921 168680 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415151 168680 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038106 217718 0 None 16 2 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1C[C@@H](O)C[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL3038099 217711 0 None 2 2 Human 9.6 pKi = 9.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57399983 78350 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956859 78350 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963149 78350 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396536 78359 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956860 78359 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963163 78359 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396540 78365 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956867 78365 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963177 78365 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105698 143124 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373459 143124 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105694 148672 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL386794 148672 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
22008895 117335 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 117335 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10996140 74450 0 None 309 2 Rat 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907652 74450 0 None 309 2 Rat 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
57393062 78352 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956869 78352 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963151 78352 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105727 90586 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220591 90586 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105742 144932 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL376866 144932 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL5280457 200847 0 None - 1 Human 9.4 pKi = 9.4 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1312 30 18 17 -4.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1Cc2ccccc2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
CHEMBL3038094 217707 0 None 8 2 Human 9.4 pKi = 9.4 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCC1 10.1021/jm950716i
CHEMBL3038095 217708 0 None 3 2 Human 9.4 pKi = 9.4 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
57403505 78420 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956865 78420 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963559 78420 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394784 78442 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956871 78442 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963658 78442 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10463758 145649 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378189 145649 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10101294 146932 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380273 146932 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44412007 83986 1 None -1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 83986 1 None -1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
10396101 91117 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221683 91117 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441167 103763 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL266493 103763 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10101294 146932 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 146932 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10102296 168681 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415152 168681 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44316161 168295 0 None -1 2 Human 9.4 pKi = 9.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1043 25 12 16 -4.0 NCCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O 10.1021/jm990961s
CHEMBL412824 168295 0 None -1 2 Human 9.4 pKi = 9.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1043 25 12 16 -4.0 NCCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O 10.1021/jm990961s
122189902 130201 0 None 13489 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 130201 0 None 13489 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
3812 7504 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
439201 7504 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
649 7504 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL406291 7504 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB12126 7504 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
5312119 7505 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
680 7505 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
CHEMBL308468 7505 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
5312119 7505 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
680 7505 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
CHEMBL308468 7505 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
57401782 78361 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956873 78361 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963165 78361 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11600186 85072 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210788 85072 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
16105701 90744 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220693 90744 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
10350966 91399 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222167 91399 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2370040 216552 0 None - 1 Guinea pig 9.3 pKi = 9.3 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None C[C@@](Cc1ccccc1)(NC(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44337490 15940 0 None - 1 Human 9.2 pKi = 9.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 307 3 0 4 1.5 CC(=O)CN1CN(C2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL110188 15940 0 None - 1 Human 9.2 pKi = 9.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 307 3 0 4 1.5 CC(=O)CN1CN(C2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
10556495 174718 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL2112044 174718 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL431562 174718 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
10556495 174718 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112044 174718 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL431562 174718 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
44340859 16815 0 None - 1 Guinea pig 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 16815 0 None - 1 Guinea pig 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
57393060 78362 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956851 78362 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963174 78362 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398328 78443 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956874 78443 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963659 78443 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 82701 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL205093 82701 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10463818 146050 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379063 146050 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10010104 148052 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383167 148052 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10439868 82701 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 82701 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10463883 90608 0 None -25 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 90608 0 None -25 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079793 100895 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL249235 100895 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105729 143712 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374273 143712 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079797 144375 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375576 144375 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 144409 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 144409 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10010104 148052 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 148052 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
3812 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
439201 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
649 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL406291 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB12126 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
3812 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
439201 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
649 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
CHEMBL406291 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
DB12126 7504 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
71450888 85568 0 None 8 2 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2112698 85568 0 None 8 2 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL5284501 201035 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1228 31 19 18 -5.9 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
44355233 173435 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL428148 173435 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
70683601 81293 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL 1270 33 15 15 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00062a018
CHEMBL2028979 81293 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL 1270 33 15 15 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00062a018
667 8754 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
6918173 8754 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
71364 8754 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
CHEMBL2028850 8754 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
DB06196 8754 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
9987299 85376 0 None 13 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 85376 0 None 13 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
57401780 78354 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956872 78354 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963153 78354 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391277 78441 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956868 78441 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963652 78441 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
44412007 83986 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207939 83986 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
10102599 148182 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383989 148182 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10418701 103877 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL267493 103877 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
122189902 130201 0 None 13489 2 Guinea pig 9.0 pKi = 9 Binding
Binding affinity to B2R in guinea pig ileum membranesBinding affinity to B2R in guinea pig ileum membranes
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 130201 0 None 13489 2 Guinea pig 9.0 pKi = 9 Binding
Binding affinity to B2R in guinea pig ileum membranesBinding affinity to B2R in guinea pig ileum membranes
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
57401776 78351 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956866 78351 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963150 78351 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10349694 83358 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206312 83358 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10418252 145669 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378237 145669 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10373970 144392 0 None -5 2 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 144392 0 None -5 2 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
3812 7504 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
439201 7504 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
649 7504 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
CHEMBL406291 7504 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
DB12126 7504 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
10055774 83478 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206474 83478 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10441194 91397 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222156 91397 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44341039 16283 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 16283 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
18941145 16735 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 16735 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
22008892 116939 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL323693 116939 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
11136263 85361 0 None 43 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112221 85361 0 None 43 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2370010 216546 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N1)C(=O)O 10.1021/jm00069a016
10418495 84650 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209346 84650 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10260476 84772 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209719 84772 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
9988753 90607 0 None -7 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 90607 0 None -7 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10788314 126745 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 421 7 4 5 3.7 NC(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL349817 126745 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 421 7 4 5 3.7 NC(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
18941160 16687 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 16687 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10010669 83586 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206938 83586 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44276460 106015 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.6 CCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL281706 106015 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.6 CCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
11527838 85133 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL211017 85133 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
11513471 145425 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
CHEMBL377612 145425 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
9987299 85376 0 None -13 2 Rat 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 85376 0 None -13 2 Rat 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44410425 103914 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL267822 103914 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
11699718 83862 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 524 9 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207465 83862 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 524 9 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN)c3Cl)c2n1 10.1021/jm060137l
11513163 84551 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 7 2 6 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209130 84551 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 7 2 6 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCCC4)c3Cl)c2n1 10.1021/jm060137l
44320402 21120 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162589 21120 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1200092 21120 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
44347466 21108 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1162799 21108 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1200034 21108 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
44347552 18950 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1184218 18950 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL339723 18950 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
2324360 63967 12 None - 1 Rat 4.0 pKi = 4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 257 4 3 2 2.7 S=C(NCc1ccccc1)NNc1ccccc1 10.1021/jm991155o
CHEMBL164968 63967 12 None - 1 Rat 4.0 pKi = 4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 257 4 3 2 2.7 S=C(NCc1ccccc1)NNc1ccccc1 10.1021/jm991155o
44215785 102309 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 557 8 0 7 5.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL25751 102309 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 557 8 0 7 5.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
101653258 20554 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320402 20554 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195447 20554 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554592 20554 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44355241 175503 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL436963 175503 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
118719116 122222 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL3350763 122222 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
44346315 20613 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1195864 20613 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL555493 20613 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44346282 19120 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1185367 19120 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL409910 19120 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
9919335 113362 1 None -489 2 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL 922 22 9 13 -2.1 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC2(CC1)C(=O)N(CC(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc3ccccc3N(CC(=O)O)C1=O)CN2CCc1ccccc1 10.1021/jm990962k
CHEMBL3142392 113362 1 None -489 2 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL 922 22 9 13 -2.1 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC2(CC1)C(=O)N(CC(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc3ccccc3N(CC(=O)O)C1=O)CN2CCc1ccccc1 10.1021/jm990962k
11050762 74449 0 None -5248 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907651 74449 0 None -5248 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
71456185 85304 0 None - 1 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL2111994 85304 0 None - 1 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL3038100 217712 0 None -14 2 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None N=C(N)NCCCCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL2372276 216985 0 None 3 3 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950716i
1016 10519 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2561 10519 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2733526 10519 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
5384 10519 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
CHEMBL83 10519 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
DB00675 10519 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
22288574 106354 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 606 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL283824 106354 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 606 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11549560 85046 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 4 7 4.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(C(N)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210708 85046 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 4 7 4.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(C(N)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5268614 200354 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1024 24 13 13 -3.9 N=C(N)NCCCC(NC(=O)CN1CCCCC2(CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O)C(=O)O 10.1021/acs.jmedchem.6b01029
44276438 106221 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 580 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL282981 106221 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 580 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44355038 168473 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1065 25 13 15 -5.1 NC(N)=NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901529
CHEMBL413386 168473 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1065 25 13 15 -5.1 NC(N)=NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901529
CHEMBL5279008 200789 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1049 25 14 14 -3.7 N=C(N)NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)CSc2ccccc21)C(=O)O 10.1021/acs.jmedchem.6b01029
70695304 84225 0 None 17 2 Human 6.9 pKi = 6.9 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 556 8 2 6 4.0 Cc1ccc2cccc(OCc3cc(S(=O)(=O)N4CCC[C@H]4C(=O)NCC4CCNCC4)ccc3Cl)c2n1 10.1021/jm2016057
CHEMBL2087027 84225 0 None 17 2 Human 6.9 pKi = 6.9 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 556 8 2 6 4.0 Cc1ccc2cccc(OCc3cc(S(=O)(=O)N4CCC[C@H]4C(=O)NCC4CCNCC4)ccc3Cl)c2n1 10.1021/jm2016057
44346367 17023 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cnc2ccccc2c1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160972 17023 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cnc2ccccc2c1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
18941161 16501 0 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 16501 0 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
11342079 168565 0 None - 1 Human 4.9 pKi = 4.9 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL414091 168565 0 None - 1 Human 4.9 pKi = 4.9 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
44355196 148302 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1328 35 16 18 -6.0 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@](Cc2ccccc2)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)C1Cc1ccccc1)C(=O)O 10.1021/jm9901531
CHEMBL384617 148302 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1328 35 16 18 -6.0 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@](Cc2ccccc2)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)C1Cc1ccccc1)C(=O)O 10.1021/jm9901531
CHEMBL3038101 217713 0 None 1 2 Human 7.8 pKi = 7.8 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
57393602 74454 0 None -3 2 Rat 7.8 pKi = 7.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907656 74454 0 None -3 2 Rat 7.8 pKi = 7.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2370011 216547 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N[C@@H](Cc2ccccc2)C(=O)N1)C(=O)O 10.1021/jm00069a016
44346372 19876 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190356 19876 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540643 19876 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
71456177 85281 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
CHEMBL2111891 85281 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
11284303 73116 0 None 2 2 Human 5.9 pKi = 5.9 Binding
Binding affinity for Bradykinin receptor B2 expressed in COS7 cellsBinding affinity for Bradykinin receptor B2 expressed in COS7 cells
ChEMBL 553 15 1 7 4.7 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm049747g
CHEMBL185068 73116 0 None 2 2 Human 5.9 pKi = 5.9 Binding
Binding affinity for Bradykinin receptor B2 expressed in COS7 cellsBinding affinity for Bradykinin receptor B2 expressed in COS7 cells
ChEMBL 553 15 1 7 4.7 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm049747g
44276461 105049 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL27461 105049 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
10556495 174718 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112044 174718 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL431562 174718 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
10770256 63939 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 627 16 3 8 4.5 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL164754 63939 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 627 16 3 8 4.5 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
44276793 106298 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 9 0 6 7.0 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL283394 106298 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 9 0 6 7.0 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11467345 168730 0 None -489 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL415629 168730 0 None -489 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
11549562 84287 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 3 7 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(N(C)C)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208738 84287 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 3 7 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(N(C)C)cc4)c3Cl)c2n1 10.1021/jm060137l
11549335 146927 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 9 3 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380260 146927 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 9 3 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
11621618 146935 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 538 10 3 6 4.0 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380282 146935 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 538 10 3 6 4.0 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
11621850 173097 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 4 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4c[nH]cn4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL427217 173097 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 4 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4c[nH]cn4)c3Cl)c2n1 10.1021/jm060137l
51351563 65282 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL1683738 65282 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
71450890 85570 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
CHEMBL2112709 85570 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
44340818 117386 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 117386 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10662116 63323 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 302 5 3 4 3.0 O=[N+]([O-])c1ccccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
CHEMBL163956 63323 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 302 5 3 4 3.0 O=[N+]([O-])c1ccccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
16108965 168109 0 None -1000 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
CHEMBL412552 168109 0 None -1000 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
71459890 85280 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2111889 85280 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2370038 216551 0 None - 1 Guinea pig 5.8 pKi = 5.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(CC(=O)N(C)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N 10.1021/jm00069a016
44276753 172106 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 7 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C(C)(C)C)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL423482 172106 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 7 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C(C)(C)C)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10327403 85360 0 None -63 2 Rat 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 85360 0 None -63 2 Rat 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44276287 171598 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 5 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C5CCCCC5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL421863 171598 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 5 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C5CCCCC5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44346451 17026 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 695 10 3 3 8.4 O=C(NC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160979 17026 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 695 10 3 3 8.4 O=C(NC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44355256 164002 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1148 31 16 17 -8.0 NC(N)=NCCC[C@H](NC(=O)CN1CCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL407626 164002 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1148 31 16 17 -8.0 NC(N)=NCCC[C@H](NC(=O)CN1CCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
672 9047 21 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
6918284 9047 21 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2105864 9047 21 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06549 9047 21 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
44276550 104073 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 570 9 0 6 6.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26908 104073 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 570 9 0 6 6.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL2370748 216697 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None Cc1ccc(C[C@@H](CN[C@@H](CCCN=C(N)N)C(=O)O)NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)cc1 10.1021/jm9901531
11577748 84872 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 10 4 6 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210217 84872 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 10 4 6 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11505970 84956 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 656 13 5 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210472 84956 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 656 13 5 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5272490 200505 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1210 31 19 17 -6.4 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H]1Cc2ccccc2CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
11585604 83902 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 11 2 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN(C)C)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207692 83902 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 11 2 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN(C)C)c3Cl)c2n1 10.1021/jm060137l
11672243 84973 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 658 14 3 7 5.8 COc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
CHEMBL210524 84973 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 658 14 3 7 5.8 COc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
11600235 145189 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 642 13 3 6 6.1 Cc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
CHEMBL377370 145189 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 642 13 3 6 6.1 Cc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
11707335 146097 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 11 3 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379259 146097 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 11 3 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCCN)c3Cl)c2n1 10.1021/jm060137l
11672186 146473 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 628 13 3 6 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379806 146473 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 628 13 3 6 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5266765 200270 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1212 31 19 18 -6.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1COc2ccccc2N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
44355427 148655 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1212 31 16 18 -7.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1COc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL386697 148655 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1212 31 16 18 -7.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1COc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
22008929 16522 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 16522 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10056816 84524 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209038 84524 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL3038096 217709 0 None 6 2 Human 8.6 pKi = 8.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10327403 85360 0 None 63 2 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 85360 0 None 63 2 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9851817 16453 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 16453 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44340760 117285 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 117285 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL2372276 216985 0 None 3 3 Human 7.7 pKi = 7.7 Binding
Displacement of radiolabeled NPC 567 from human bradykinin B2 receptorDisplacement of radiolabeled NPC 567 from human bradykinin B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm8007618
22288598 103942 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 642 9 0 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(=O)N(C)C)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26810 103942 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 642 9 0 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(=O)N(C)C)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44355288 103549 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1224 33 16 17 -6.8 NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)N1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL264712 103549 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1224 33 16 17 -6.8 NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)N1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
44346465 18205 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1180311 18205 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL121350 18205 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
44346306 17019 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160968 17019 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 17020 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 17020 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 17020 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
9826248 40856 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 439 8 3 3 3.7 N=C(N)NCCCCN1C(=O)C(Cc2ccccc2)N=C(c2ccccc2)c2ccccc21 10.1016/s0960-894x(99)00015-3
CHEMBL142515 40856 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 439 8 3 3 3.7 N=C(N)NCCCCN1C(=O)C(Cc2ccccc2)N=C(c2ccccc2)c2ccccc21 10.1016/s0960-894x(99)00015-3
CHEMBL3038103 217715 0 None 61 2 Human 7.6 pKi = 7.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1)C1CCCC1 10.1021/jm950716i
44276711 103706 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 571 8 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26604 103706 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 571 8 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
15952860 106024 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 596 8 0 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL281756 106024 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 596 8 0 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11050689 109044 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 678 15 4 10 3.8 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL303258 109044 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 678 15 4 10 3.8 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
44276375 103495 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 585 9 0 5 7.4 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)Cc5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26422 103495 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 585 9 0 5 7.4 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)Cc5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276380 106195 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL28282 106195 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44320404 19895 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190474 19895 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540896 19895 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL5267275 200294 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1250 30 18 17 -5.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1CCC[C@]12Cc1ccccc1CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C2=O 10.1021/acs.jmedchem.6b01029
11679144 84071 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 10 3 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208223 84071 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 10 3 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
11636121 145789 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 7 2 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378567 145789 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 7 2 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCC4)c3Cl)c2n1 10.1021/jm060137l
44412412 175564 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 550 7 2 6 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL437491 175564 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 550 7 2 6 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
44346682 21015 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1162798 21015 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1199421 21015 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320404 21121 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
CHEMBL1162590 21121 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
CHEMBL1200093 21121 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
CHEMBL5268614 200354 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1024 24 13 13 -3.9 N=C(N)NCCCC(NC(=O)CN1CCCCC2(CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O)C(=O)O 10.1021/acs.jmedchem.6b01029
11707528 84546 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 621 11 2 7 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCN(C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209117 84546 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 621 11 2 7 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCN(C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5284537 201036 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1032 25 14 13 -4.2 N=C(N)NCCC[C@H](NC(=O)CN1Cc2ccccc2C[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O)C(=O)O 10.1021/acs.jmedchem.6b01029
11657717 146845 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 594 10 2 7 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380045 146845 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 594 10 2 7 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
10876210 85359 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 691 13 4 8 4.5 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c(Cl)c1 10.1021/jm0111088
CHEMBL2112219 85359 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 691 13 4 8 4.5 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c(Cl)c1 10.1021/jm0111088
44346347 17021 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cccc2ccncc12)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160970 17021 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cccc2ccncc12)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44346416 19874 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190354 19874 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540641 19874 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL2370042 216554 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(C(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44337466 12187 0 None - 1 Human 7.6 pKi = 7.6 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 267 4 0 4 0.6 CCCN1CN(CC(C)=O)C(=O)C12CCN(C)CC2 10.1021/jm950676i
CHEMBL107234 12187 0 None - 1 Human 7.6 pKi = 7.6 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 267 4 0 4 0.6 CCCN1CN(CC(C)=O)C(=O)C12CCN(C)CC2 10.1021/jm950676i
44276482 106279 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL283295 106279 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
44346410 20555 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195448 20555 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554593 20555 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44215784 106774 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 566 8 0 6 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL286710 106774 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 566 8 0 6 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44276513 106746 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 638 11 0 6 8.3 CCCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL286520 106746 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 638 11 0 6 8.3 CCCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
57395311 74453 0 None 2 2 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907655 74453 0 None 2 2 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44214279 16488 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 16488 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL5268547 200349 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1250 30 18 17 -5.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1CCC[C@@]12Cc1ccccc1CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C2=O 10.1021/acs.jmedchem.6b01029
15388873 121509 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL333832 121509 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44341214 117207 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 117207 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
11506007 84786 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209773 84786 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
10008626 145456 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377800 145456 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL2370028 216549 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(CC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N 10.1021/jm00069a016
22288562 169733 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 8 1 6 6.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL417474 169733 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 8 1 6 6.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL2370035 216550 0 None - 1 Guinea pig 5.5 pKi = 5.5 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CC(NC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@](C)(Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44276439 103739 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 546 9 0 6 6.3 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26629 103739 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 546 9 0 6 6.3 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44276474 104166 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 591 9 0 6 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26976 104166 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 591 9 0 6 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10504589 63951 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 471 9 4 6 3.5 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccccc2)ccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
CHEMBL164848 63951 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 471 9 4 6 3.5 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccccc2)ccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
44346389 17024 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 497 7 3 3 6.0 O=C(Nc1cccnc1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160975 17024 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 497 7 3 3 6.0 O=C(Nc1cccnc1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL5266183 200251 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1210 31 19 17 -6.4 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1Cc2ccccc2CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
11614670 84429 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 3 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccoc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208859 84429 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 3 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccoc4)c3Cl)c2n1 10.1021/jm060137l
11571204 145488 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 10 2 6 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCCCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377966 145488 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 10 2 6 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCCCC4)c3Cl)c2n1 10.1021/jm060137l
44410526 90031 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL218749 90031 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
44316621 88891 0 None -57 2 Human 6.5 pKi = 6.5 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1091 24 13 15 -4.9 NC(N)=NCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
CHEMBL216618 88891 0 None -57 2 Human 6.5 pKi = 6.5 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1091 24 13 15 -4.9 NC(N)=NCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
101653256 19875 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320170 19875 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190355 19875 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540642 19875 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44298960 202417 0 None - 1 Human 7.5 pKi = 7.5 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
CHEMBL55632 202417 0 None - 1 Human 7.5 pKi = 7.5 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
44346104 18196 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
CHEMBL1180289 18196 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
CHEMBL120282 18196 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
44320170 21064 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162585 21064 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1199851 21064 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
22288578 105888 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 649 9 0 7 6.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(C)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL280869 105888 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 649 9 0 7 6.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(C)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10930680 74452 0 None -6 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907654 74452 0 None -6 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
10100960 23261 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL123548 23261 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL333705 23261 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL539629 23261 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
10100960 23261 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL123548 23261 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL333705 23261 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL539629 23261 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
44346418 20530 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195322 20530 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554254 20530 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
11215913 143317 0 None -26915 2 Human 4.5 pKi = 4.5 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
CHEMBL373654 143317 0 None -26915 2 Human 4.5 pKi = 4.5 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
44276975 103290 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL 1081 34 13 12 -0.8 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2C1C(=O)N1CC(C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2CCCCC21 10.1021/jm00035a015
CHEMBL262639 103290 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL 1081 34 13 12 -0.8 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2C1C(=O)N1CC(C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2CCCCC21 10.1021/jm00035a015
90663066 113365 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assayCompound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142595 113365 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assayCompound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
22288581 106059 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 5 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)[nH]4)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL281951 106059 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 5 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)[nH]4)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
9830551 106824 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 620 9 0 6 7.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL287018 106824 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 620 9 0 6 7.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10571699 63926 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 378 6 3 4 4.6 O=[N+]([O-])c1ccccc1N/N=C(/S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
CHEMBL164636 63926 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 378 6 3 4 4.6 O=[N+]([O-])c1ccccc1N/N=C(/S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
22288602 106505 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL284865 106505 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
11707423 84806 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 580 11 4 6 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209873 84806 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 580 11 4 6 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11592927 146055 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 629 13 3 7 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccn4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379083 146055 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 629 13 3 7 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccn4)c3Cl)c2n1 10.1021/jm060137l
11636064 84795 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 553 11 2 6 4.6 COCCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
CHEMBL209819 84795 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 553 11 2 6 4.6 COCCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
11498691 85028 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 646 13 3 6 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(F)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210662 85028 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 646 13 3 6 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(F)cc4)c3Cl)c2n1 10.1021/jm060137l
9916936 106487 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL284727 106487 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10790025 64232 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 457 7 4 6 3.2 NS(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL165627 64232 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 457 7 4 6 3.2 NS(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
44316620 8902 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
656 8902 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL408846 8902 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
57393602 74454 0 None 3 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907656 74454 0 None 3 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44320168 17020 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160969 17020 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL444322 17020 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 17020 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 17020 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 17020 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
44346412 19872 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190352 19872 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540639 19872 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
70688994 84226 0 None -18 2 Human 4.4 pKi = 4.4 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 433 5 2 4 2.6 Cc1c(Cl)ccc(S(=O)(=O)N2CCC[C@H]2C(=O)NCC2CCNCC2)c1Cl 10.1021/jm2016057
CHEMBL2087028 84226 0 None -18 2 Human 4.4 pKi = 4.4 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 433 5 2 4 2.6 Cc1c(Cl)ccc(S(=O)(=O)N2CCC[C@H]2C(=O)NCC2CCNCC2)c1Cl 10.1021/jm2016057
44276459 103132 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 652 11 0 6 8.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4CCC(C)C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26160 103132 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 652 11 0 6 8.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4CCC(C)C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
90663068 113366 0 None - 1 Human 7.4 pKi = 7.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptorCompound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptor
ChEMBL 1095 35 13 12 -0.3 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142597 113366 0 None - 1 Human 7.4 pKi = 7.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptorCompound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptor
ChEMBL 1095 35 13 12 -0.3 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
44340964 16479 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 16479 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10482991 107426 0 None - 1 Human 7.3 pKi = 7.3 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
CHEMBL292181 107426 0 None - 1 Human 7.3 pKi = 7.3 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
44346414 20531 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195323 20531 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554255 20531 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44276666 105393 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 639 8 0 5 8.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(F)(F)F)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL27701 105393 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 639 8 0 5 8.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(F)(F)F)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44355289 168683 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL415209 168683 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
16108960 176038 0 None -30902 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL441188 176038 0 None -30902 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
44300140 108386 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 526 8 4 3 6.1 O=C(Nc1ccc(CO)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL298832 108386 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 526 8 4 3 6.1 O=C(Nc1ccc(CO)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44214619 117382 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 117382 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
10930680 74452 0 None 6 2 Rat 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907654 74452 0 None 6 2 Rat 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL5278855 200780 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1046 25 14 13 -3.8 C[C@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)N1Cc2ccccc2C[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O 10.1021/acs.jmedchem.6b01029
44276716 106486 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 622 10 0 6 7.6 C=CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL284726 106486 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 622 10 0 6 7.6 C=CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
44355287 168658 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL415032 168658 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
122189855 130190 0 None -75 3 Rat 5.3 pKi = 5.3 Binding
Displacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616879 130190 0 None -75 3 Rat 5.3 pKi = 5.3 Binding
Displacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
44346361 17022 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 536 7 4 3 6.5 O=C(Nc1nc2ccccc2[nH]1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160971 17022 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 536 7 4 3 6.5 O=C(Nc1nc2ccccc2[nH]1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
10742229 127047 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 451 9 4 8 2.7 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccco2)ccc1N/N=C(/S)NCc1ccco1 10.1021/jm991155o
CHEMBL352459 127047 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 451 9 4 8 2.7 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccco2)ccc1N/N=C(/S)NCc1ccco1 10.1021/jm991155o
44276455 105153 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL27530 105153 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
44346306 17019 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160968 17019 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 17020 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 17020 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 17020 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
44276487 106775 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(NC(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL286711 106775 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(NC(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
16108967 91119 0 None -147 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 541 10 2 4 5.6 O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NCc1ccc(CN2CCCCC2)cc1 10.1021/jm061224g
CHEMBL221691 91119 0 None -147 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 541 10 2 4 5.6 O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NCc1ccc(CN2CCCCC2)cc1 10.1021/jm061224g
10461651 106149 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL282562 106149 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
16108969 89806 0 None -239883 2 Human 4.2 pKi = 4.2 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL218152 89806 0 None -239883 2 Human 4.2 pKi = 4.2 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL5271423 200462 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1312 30 18 17 -4.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
CHEMBL3038105 217717 0 None 3 2 Human 6.2 pKi = 6.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)O)Cc1ccccc1 10.1021/jm950716i
71450888 85568 0 None -8 2 Rat 8.2 pKi = 8.2 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2112698 85568 0 None -8 2 Rat 8.2 pKi = 8.2 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
44355234 103233 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1242 31 16 18 -6.2 Cc1ccc2c(c1)SCC(NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CC(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm9901531
CHEMBL262313 103233 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1242 31 16 18 -6.2 Cc1ccc2c(c1)SCC(NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CC(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm9901531
22008916 16534 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 16534 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44337425 116654 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 315 3 0 4 1.7 CC(=O)CN1CN(c2ccc(C)cc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL323421 116654 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 315 3 0 4 1.7 CC(=O)CN1CN(c2ccc(C)cc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
44340951 16774 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 16774 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
44337476 14900 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 321 4 0 4 1.7 CC(=O)CN1CN(CC2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL109172 14900 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 321 4 0 4 1.7 CC(=O)CN1CN(CC2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
132927 10856 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
138398059 10856 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
677 10856 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
CHEMBL294453 10856 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
CHEMBL551291 10856 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
101005081 19873 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44346317 19873 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190353 19873 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540640 19873 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
132928 21069 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL1162586 21069 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL1199865 21069 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
132928 21069 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162586 21069 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1199865 21069 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
90662943 113361 0 None -1778 2 Human 7.2 pKi = 7.2 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1192 30 14 17 -4.3 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
CHEMBL3142391 113361 0 None -1778 2 Human 7.2 pKi = 7.2 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1192 30 14 17 -4.3 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
11650337 145465 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 523 7 3 5 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377835 145465 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 523 7 3 5 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11542210 84384 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 608 11 2 7 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208807 84384 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 608 11 2 7 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
11136263 85361 0 None -43 2 Rat 7.2 pKi = 7.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112221 85361 0 None -43 2 Rat 7.2 pKi = 7.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
10952583 74455 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 694 14 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3-c3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907657 74455 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 694 14 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3-c3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
57395311 74453 0 None -2 2 Rat 6.2 pKi = 6.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907655 74453 0 None -2 2 Rat 6.2 pKi = 6.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9915727 102300 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 556 8 0 6 6.4 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL25745 102300 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 556 8 0 6 6.4 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
10886849 74451 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 655 14 4 7 3.5 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC(c2ccccc2)c2ccccc2)c(Cl)c1 10.1021/jm0111088
CHEMBL1907653 74451 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 655 14 4 7 3.5 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC(c2ccccc2)c2ccccc2)c(Cl)c1 10.1021/jm0111088
44337489 16002 0 None - 1 Human 8.1 pKi = 8.1 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 301 3 0 4 1.3 CC(=O)CN1CN(c2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL110652 16002 0 None - 1 Human 8.1 pKi = 8.1 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 301 3 0 4 1.3 CC(=O)CN1CN(c2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL2392354 217194 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None N=C(N)NCCC[C@H](N)C(=O)N[C@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1016/j.ejmech.2013.01.044
11527906 146896 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 670 13 5 7 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380086 146896 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 670 13 5 7 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
45266122 19877 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190357 19877 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540644 19877 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44346679 19894 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190473 19894 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540895 19894 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
10542327 64187 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 301 5 2 3 3.2 O=[N+]([O-])c1ccccc1C/N=C(\S)NCc1ccccc1 10.1021/jm991155o
CHEMBL165240 64187 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 301 5 2 3 3.2 O=[N+]([O-])c1ccccc1C/N=C(\S)NCc1ccccc1 10.1021/jm991155o
44276840 106751 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1cccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)c1 10.1016/s0960-894x(03)00104-5
CHEMBL286556 106751 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1cccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)c1 10.1016/s0960-894x(03)00104-5
44276488 103984 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 597 8 0 7 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26847 103984 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 597 8 0 7 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276624 103627 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 605 8 0 5 7.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26532 103627 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 605 8 0 5 7.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276599 103183 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 650 9 1 7 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(N)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26192 103183 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 650 9 1 7 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(N)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44346387 21107 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1162797 21107 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1200033 21107 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
176 7186 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2157 7186 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2566 7186 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
CHEMBL633 7186 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
DB01118 7186 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
10373002 145089 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL121565 145089 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL377100 145089 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
10373002 145089 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL121565 145089 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL377100 145089 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
44355257 173241 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL427805 173241 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
5312119 7505 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
680 7505 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
CHEMBL308468 7505 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
11650783 59203 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 14 3 8 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(S(C)(=O)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL159066 59203 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 14 3 8 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(S(C)(=O)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
11636119 84853 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 8 3 6 4.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210100 84853 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 8 3 6 4.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
11686399 146915 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 644 13 4 7 5.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380206 146915 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 644 13 4 7 5.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5285641 201085 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1032 25 14 13 -4.2 N=C(N)NCCC[C@H](NC(=O)CN1Cc2ccccc2CC(NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O)C(=O)O 10.1021/acs.jmedchem.6b01029
11527892 146306 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 662 13 3 6 6.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(Cl)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379541 146306 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 662 13 3 6 6.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(Cl)cc4)c3Cl)c2n1 10.1021/jm060137l
11671905 84534 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 539 10 2 6 4.2 COCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
CHEMBL209068 84534 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 539 10 2 6 4.2 COCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
11513104 84943 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 557 8 2 5 6.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)Nc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210427 84943 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 557 8 2 5 6.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)Nc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
10895913 16641 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 16641 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL3038102 217714 0 None 5 2 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)Cc1ccccc1 10.1021/jm950716i
44347466 21108 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1162799 21108 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1200034 21108 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
44347757 18219 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1180347 18219 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL123124 18219 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL2370041 216553 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CC(NC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44346449 17025 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 619 9 2 3 7.1 O=C([C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1)N(Cc1ccccc1)C1CN2CCC1CC2 10.1016/0960-894X(95)00035-R
CHEMBL1160978 17025 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 619 9 2 3 7.1 O=C([C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1)N(Cc1ccccc1)C1CN2CCC1CC2 10.1016/0960-894X(95)00035-R
118719116 122222 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL3350763 122222 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
44276841 102304 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccccc1C(=O)c1ccc(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)n1C 10.1016/s0960-894x(03)00104-5
CHEMBL25748 102304 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccccc1C(=O)c1ccc(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)n1C 10.1016/s0960-894x(03)00104-5
CHEMBL5274916 200608 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1405 31 20 19 -4.2 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@H]1CSSC[C@@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC1=O 10.1021/acs.jmedchem.6b01029
10005078 40541 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL142260 40541 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
15388870 117410 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL325742 117410 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL3085458 217767 6 None -398 2 Human 8.0 pKi = 8.0 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990962k
CHEMBL3085458 217767 6 None -398 2 Human 8.0 pKi = 8.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
44341060 16332 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112360 16332 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
122189902 130201 0 None -13489 2 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 130201 0 None -13489 2 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
44276667 105394 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 601 9 0 6 7.2 COc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL27702 105394 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 601 9 0 6 7.2 COc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
44361937 176183 0 None - 1 Human 5.0 pKi = 5.0 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 459 5 3 3 5.1 N=C(N)Nc1ccc(N2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)cc1 10.1016/s0960-894x(99)00015-3
CHEMBL442294 176183 0 None - 1 Human 5.0 pKi = 5.0 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 459 5 3 3 5.1 N=C(N)Nc1ccc(N2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)cc1 10.1016/s0960-894x(99)00015-3
10996140 74450 0 None -309 2 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907652 74450 0 None -309 2 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
3812 7504 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
439201 7504 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
649 7504 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
CHEMBL406291 7504 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
DB12126 7504 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
122173054 224513 0 None -1 6 Rat 8.0 pKi = 8 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
122173054 224513 0 None -1 6 Human 8.0 pKi = 8.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
3075702 224111 0 3H-NPC 17731 -2 37 Human 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 198 3 1 3 1.5 C1CNC1COC2=CN=C(C=C2)Cl None
243 9976 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3052762 9976 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3502 9976 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
CHEMBL117287 9976 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
DB06480 9976 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
44208932 147485 7 UNDEFINED -89125 37 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 475 5 1 3 6.8 Cc1ccc(Cn2nc(C(=O)NC3C4(C)CCC(C4)C3(C)C)cc2-c2ccc(Cl)c(C)c2)cc1 None
CHEMBL381689 147485 7 UNDEFINED -89125 37 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 475 5 1 3 6.8 Cc1ccc(Cn2nc(C(=O)NC3C4(C)CCC(C4)C3(C)C)cc2-c2ccc(Cl)c(C)c2)cc1 None
1973 210262 15 3H-NPC 17731 -3 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
CHEMBL1394464 210262 15 3H-NPC 17731 -3 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
CHEMBL66089 210262 15 3H-NPC 17731 -3 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
None 223272 0 3H-BRADYKININ -10471285 17 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 372 2 1 3 4.4 CC(C)(C)C1=CC=C(C=C1)NC(=O)N2CCN(CC2)C3=C(C=CC=N3)Cl None
1016 10519 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
2561 10519 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
2733526 10519 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
5384 10519 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
CHEMBL83 10519 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
DB00675 10519 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
176 7186 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
2157 7186 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
2566 7186 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
CHEMBL633 7186 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
DB01118 7186 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
122173054 224513 0 None -1 6 Mouse 8.0 pKi = 8.0 Binding
NoneNone
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
122173054 224513 0 None -1 6 Guinea pig 8.0 pKi = 8 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
12421 8181 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 32636746
12421 8181 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 35086057
154623230 8181 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 32636746
154623230 8181 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 35086057
11159 7878 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.
Guide to Pharmacology 533 9 1 7 5.1 FC(OCC(=O)N[C@H](c1cc(F)cc(c1COc1cccc2c1nc(C)cc2c1ncnn1C)Cl)C)F 32636746
138634054 7878 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.
Guide to Pharmacology 533 9 1 7 5.1 FC(OCC(=O)N[C@H](c1cc(F)cc(c1COc1cccc2c1nc(C)cc2c1ncnn1C)Cl)C)F 32636746
667 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
6918173 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
71364 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
CHEMBL2028850 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
DB06196 8754 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
679 7202 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
9831652 7202 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
CHEMBL2107725 7202 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
DB05038 7202 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
670 8901 0 None 8 2 Rat 10.1 pKi None 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
667 8754 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
6918173 8754 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
71364 8754 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
CHEMBL2028850 8754 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
DB06196 8754 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
5312119 7505 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
680 7505 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
CHEMBL308468 7505 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
658 9647 0 None -3981 2 Human 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
132927 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
132927 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
138398059 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
138398059 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
677 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
677 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
CHEMBL294453 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
CHEMBL294453 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
CHEMBL551291 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
CHEMBL551291 10856 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
5311114 8469 8 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
668 8469 8 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
CHEMBL99869 8469 8 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
679 7202 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
9831652 7202 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
CHEMBL2107725 7202 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
DB05038 7202 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
672 9047 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
672 9047 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
6918284 9047 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
6918284 9047 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
CHEMBL2105864 9047 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
CHEMBL2105864 9047 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
DB06549 9047 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
DB06549 9047 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
3081308 9646 0 None 15 2 Human 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
657 9646 0 None 15 2 Human 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
44316620 8902 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
656 8902 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
CHEMBL408846 8902 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
653 7353 0 None -1 4 Mouse 9.0 pKi None 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9276157
653 7353 0 None 1 4 Human 9.1 pKi None 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8856115
653 7353 0 None 1 4 Human 9.1 pKi None 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9276157
670 8901 0 None -8 2 Human 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
5312119 7505 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
680 7505 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
CHEMBL308468 7505 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
667 8754 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
6918173 8754 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
71364 8754 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL2028850 8754 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB06196 8754 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267