Initializing potency table...
Ligand source activities (1 row/activity)
Ligands | Receptor | Activity | Chemical information | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Common name | GPCRdb ID | Reference ligand | Vendors | Species | Assay Type | Activity Type | Activity Relation | Activity Value | p-value (-log) | Fold selectivity | Tested GPCRs | Assay Description | Source | Mol weight | Rot Bonds | H don | H acc | LogP | Smiles | DOI | |
Ligands | Receptor | Activity | Chemical information | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Common name | GPCRdb ID | Reference ligand | Vendors | Species | Assay Type | Activity Type | Activity Relation | Activity Value | p-value (-log) | Fold selectivity | Tested GPCRs | Assay Description | Source | Mol weight | Rot Bonds | H don | H acc | LogP | Smiles | DOI | |
(S)-FTY720-phosphate | 3596 | None | 37 | Human | Binding | EC50 | = | 5.01 | 8.30 | - | 6 | Agonist activity at human S1P3 receptor expressed in RBL cells by [35S]GTP-gammaS accumulation assay | ChEMBL | 387.2 | 14 | 4 | 4 | 3.32 | CCCCCCCCc1ccc(CC[C@](N)(CO)COP(=O)(O)O)cc1 | https://dx.doi.org/10.1021/acs.jmedchem.5b01512 | |
(S)-FTY720-phosphate | 3596 | None | 37 | Human | Binding | EC50 | = | 94.00 | 7.03 | - | 6 | Agonist activity at human S1P3 receptor expressed in EDG3-bla U2OS cells incubated for 18 hrs prior to GenBlazer substrate addition by beta-arrestin recruitment assay | ChEMBL | 387.2 | 14 | 4 | 4 | 3.32 | CCCCCCCCc1ccc(CC[C@](N)(CO)COP(=O)(O)O)cc1 | https://dx.doi.org/10.1016/j.bmcl.2015.11.090 | |
(S)-FTY720-phosphate | 3596 | None | 37 | Human | Binding | IC50 | = | 6.30 | 8.20 | - | 6 | Displacement of [33P]S1P from human S1P3R expressed in CHO cell membranes | ChEMBL | 387.2 | 14 | 4 | 4 | 3.32 | CCCCCCCCc1ccc(CC[C@](N)(CO)COP(=O)(O)O)cc1 | https://dx.doi.org/10.1021/ml100227q | |
BMS-986104 | 140397 | None | 11 | Human | Binding | EC50 | = | 2065.00 | 5.68 | - | 1 | Agonist activity at human S1P3 expressed in EDG3-Ga15-bla HEK293T cells incubated for 45 mins by scintillation counting based [35S]GTP-gamma-S binding assay relative to control | ChEMBL | 329.3 | 7 | 2 | 2 | 4.72 | CCCCCC[C@@H]1CCc2cc([C@H]3CC[C@](N)(CO)C3)ccc2C1 | https://dx.doi.org/10.1021/acs.jmedchem.6b01433 | |
CHEMBL1088819 | 7703 | None | 0 | Human | Binding | IC50 | = | 2000.00 | 5.70 | - | 2 | Displacement of [33P]sphingosine-1-phosphate from human S1P3 receptor expressed in HEK293T cells after 60 mins by scintillation counting | ChEMBL | 495.2 | 10 | 4 | 6 | 3.61 | C[C@](N)(COP(=O)(O)O)C(=O)Nc1ccc(OCCc2ccc(-c3ccccc3)cc2)c(C#N)c1 | https://dx.doi.org/10.1016/j.bmcl.2010.02.098 | |
CHEMBL1088820 | 7704 | None | 0 | Human | Binding | IC50 | = | 285.00 | 6.54 | - | 2 | Displacement of [33P]sphingosine-1-phosphate from human S1P3 receptor expressed in HEK293T cells after 60 mins by scintillation counting | ChEMBL | 504.1 | 10 | 4 | 5 | 4.39 | C[C@](N)(COP(=O)(O)O)C(=O)Nc1ccc(OCCc2ccc(-c3ccccc3)cc2)c(Cl)c1 | https://dx.doi.org/10.1016/j.bmcl.2010.02.098 | |
CHEMBL1089127 | 7763 | None | 0 | Human | Binding | IC50 | = | 1000.00 | 6.00 | - | 2 | Displacement of [33P]sphingosine-1-phosphate from human S1P3 receptor expressed in HEK293T cells after 60 mins by scintillation counting | ChEMBL | 548.1 | 10 | 4 | 5 | 4.50 | C[C@](N)(COP(=O)(O)O)C(=O)Nc1ccc(OCCc2ccc(-c3ccccc3)cc2)c(Br)c1 | https://dx.doi.org/10.1016/j.bmcl.2010.02.098 | |
CHEMBL1090796 | 8023 | None | 0 | Human | Binding | IC50 | = | 3800.00 | 5.42 | - | 4 | Displacement of [33P]sphingosine-1-phosphate from human S1P3 receptor expressed in HEK293T cells after 60 mins by scintillation counting | ChEMBL | 482.2 | 10 | 4 | 5 | 3.93 | C[C@](N)(COP(=O)(O)O)C(=O)Nc1ccc(C(=O)CCc2ccc(-c3ccccc3)cc2)cc1 | https://dx.doi.org/10.1016/j.bmcl.2010.02.098 | |
CHEMBL1090828 | 8032 | None | 0 | Human | Binding | IC50 | = | 700.00 | 6.16 | - | 2 | Displacement of [33P]sphingosine-1-phosphate from human S1P3 receptor expressed in HEK293T cells after 60 mins by scintillation counting | ChEMBL | 538.1 | 10 | 4 | 5 | 4.76 | C[C@](N)(COP(=O)(O)O)C(=O)Nc1ccc(OCCc2ccc(-c3ccccc3)cc2)cc1C(F)(F)F | https://dx.doi.org/10.1016/j.bmcl.2010.02.098 | |
CHEMBL1093424 | 8412 | None | 0 | Human | Binding | IC50 | = | 3250.00 | 5.49 | - | 2 | Displacement of [33P]sphingosine-1-phosphate from human S1P3 receptor expressed in HEK293T cells after 60 mins by scintillation counting | ChEMBL | 484.2 | 10 | 4 | 5 | 4.05 | Cc1cc(NC(=O)[C@@](C)(N)COP(=O)(O)O)ccc1OCCc1ccc(-c2ccccc2)cc1 | https://dx.doi.org/10.1016/j.bmcl.2010.02.098 | |
CHEMBL1093429 | 8413 | None | 0 | Human | Binding | IC50 | = | 4500.00 | 5.35 | - | 4 | Displacement of [33P]sphingosine-1-phosphate from human S1P3 receptor expressed in HEK293T cells after 60 mins by scintillation counting | ChEMBL | 538.1 | 10 | 4 | 5 | 4.76 | C[C@](N)(COP(=O)(O)O)C(=O)Nc1ccc(OCCc2ccc(-c3ccccc3)cc2)c(C(F)(F)F)c1 | https://dx.doi.org/10.1016/j.bmcl.2010.02.098 | |
CHEMBL1093823 | 8466 | None | 0 | Human | Binding | IC50 | = | 2000.00 | 5.70 | - | 4 | Displacement of [33P]sphingosine-1-phosphate from human S1P3 receptor expressed in HEK293T cells after 60 mins by scintillation counting | ChEMBL | 547.1 | 9 | 4 | 5 | 5.63 | C[C@](N)(COP(=O)(O)O)c1nc(-c2ccc(OCc3ccc(-c4ccccc4)cc3)c(C(F)(F)F)c2)c[nH]1 | https://dx.doi.org/10.1016/j.bmcl.2010.02.098 | |
CHEMBL1095833 | 8719 | None | 24 | Human | Binding | IC50 | = | 2068.00 | 5.68 | - | 4 | Displacement of [33P]S1P from human recombinant S1P3 receptor expressed in HEK cells by scintillation counting | ChEMBL | 460.1 | 8 | 2 | 6 | 4.27 | CCC/N=C1\S/C(=C\c2ccc(OC[C@@H](O)CO)c(Cl)c2)C(=O)N1c1ccccc1C | https://dx.doi.org/10.1021/jm100181s | |
CHEMBL112655 | 9627 | None | 0 | Human | Binding | IC50 | = | 68.00 | 7.17 | - | 4 | Inhibition of [33P]-S1P binding to human Sphingosine 1-phosphate receptor 3 expressed on CHO cell membranes | ChEMBL | 371.2 | 13 | 4 | 3 | 3.39 | CCCCCCCCc1ccc(CCC(N)C(O)CP(=O)(O)O)cc1 | https://dx.doi.org/10.1016/j.bmcl.2004.02.106 | |
CHEMBL113344 | 9736 | None | 0 | Human | Binding | IC50 | = | 62.00 | 7.21 | - | 4 | Inhibition of [33P]-S1P binding to human Sphingosine 1-phosphate receptor 3 expressed on CHO cell membranes | ChEMBL | 371.2 | 13 | 4 | 3 | 3.74 | CCCCCCCCc1ccc(CCC(N)CC(O)P(=O)(O)O)cc1 | https://dx.doi.org/10.1016/j.bmcl.2004.02.106 | |
CHEMBL114584 | 9939 | None | 2 | Human | Binding | IC50 | = | 510.00 | 6.29 | - | 4 | Inhibition of [33P]-S1P binding to human Sphingosine 1-phosphate receptor 3 expressed on CHO cell membranes | ChEMBL | 385.2 | 14 | 4 | 3 | 3.78 | CCCCCCCCc1ccc(CCC(N)(CO)CCP(=O)(O)O)cc1 | https://dx.doi.org/10.1016/j.bmcl.2004.02.106 | |
CHEMBL114584 | 9939 | None | 2 | Human | Binding | IC50 | = | 7.00 | 8.15 | - | 4 | Displacement of [33P]-S1P from S1P3 receptor (unknown origin) expressed in CHO cell membranes | ChEMBL | 385.2 | 14 | 4 | 3 | 3.78 | CCCCCCCCc1ccc(CCC(N)(CO)CCP(=O)(O)O)cc1 | https://dx.doi.org/10.1021/acs.jmedchem.6b01575 | |
CHEMBL114976 | 10016 | None | 0 | Human | Binding | IC50 | = | 320.00 | 6.50 | - | 4 | Inhibition of [33P]-S1P binding to human Sphingosine 1-phosphate receptor 3 expressed on CHO cell membranes | ChEMBL | 371.2 | 13 | 4 | 3 | 3.74 | CCCCCCCCc1ccc(CC[C@H](N)C[C@@H](O)P(=O)(O)O)cc1 | https://dx.doi.org/10.1016/j.bmcl.2004.02.106 | |
CHEMBL115131 | 10039 | None | 0 | Human | Binding | IC50 | = | 7600.00 | 5.12 | - | 3 | Inhibition of [33P]-S1P binding to human Sphingosine 1-phosphate receptor 3 expressed on CHO cell membranes | ChEMBL | 355.2 | 13 | 2 | 3 | 4.13 | CCCCCCCCc1ccc(CCC(N)CCS(=O)(=O)O)cc1 | https://dx.doi.org/10.1016/j.bmcl.2004.02.106 | |
CHEMBL115554 | 10108 | None | 0 | Human | Binding | IC50 | = | 18.00 | 7.75 | - | 4 | Inhibition of [33P]-S1P binding to human Sphingosine 1-phosphate receptor 3 expressed on CHO cell membranes | ChEMBL | 371.2 | 13 | 4 | 3 | 3.74 | CCCCCCCCc1ccc(CC[C@@H](N)C[C@@H](O)P(=O)(O)O)cc1 | https://dx.doi.org/10.1016/j.bmcl.2004.02.106 |
Showing 1 to 20 of 484 entries
Ligands | Receptor | Activity | Chemical information | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Common name |
GPCRdb ID |
Reference ligand |
Vendors | Species | Assay Type |
Activity Type |
Activity Relation |
Activity Value |
p-value (-log) |
Fold selectivity |
Tested GPCRs |
Assay Description |
Source | Mol weight |
Rot Bonds |
H don | H acc | LogP | Smiles | DOI | |