(+)-chlorpheniramine


SMILES CN(CC[C@H](c1ccccn1)c1ccc(cc1)Cl)C
InChIKey SOYKEARSMXGVTM-HNNXBMFYSA-N

Chemical properties

Hydrogen bond acceptors 2
Hydrogen bond donors 0
Rotatable bonds 5
Molecular weight (Da) 274.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug Yes

Sankey plot


Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
H1 HRH1 Human Histamine A pKi 6.4 7.72 8.6 Guide to Pharmacology
H1 HRH1 Human Histamine A pKi 5.0 7.68 8.6 PDSP Ki database
H1 HRH1 Guinea pig Histamine A pKi 9.3 9.33 9.36 PDSP Ki database
α1B ADA1B Rat Adrenoceptors A pKi 5.07 5.07 5.07 ChEMBL
H3 HRH3 Rat Histamine A pKi 5.0 5.0 5.0 PDSP Ki database
α1D ADA1D Human Adrenoceptors A pKi 4.78 4.78 4.78 ChEMBL
α2B ADA2B Human Adrenoceptors A pKi 5.68 5.68 5.68 ChEMBL
M5 ACM5 Human Acetylcholine (muscarinic) A pKi 6.13 6.13 6.13 ChEMBL
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 6.56 6.56 6.56 ChEMBL
H1 HRH1 Human Histamine A pKi 8.15 8.67 9.14 ChEMBL
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 6.26 6.26 6.26 ChEMBL
α2A ADA2A Human Adrenoceptors A pKi 5.12 5.12 5.12 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 5.6 5.6 5.6 ChEMBL
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 5.92 5.92 5.92 ChEMBL
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 6.48 6.48 6.48 ChEMBL
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 5.98 5.98 5.98 ChEMBL
H4 HRH4 Human Histamine A pKi 5.54 5.54 5.54 PDSP Ki database
5-HT2A 5HT2A Rat 5-Hydroxytryptamine A pKi 5.53 5.53 5.53 PDSP Ki database
5-HT2B 5HT2B Human 5-Hydroxytryptamine A pKi 8.29 8.29 8.29 Drug Central
H1 HRH1 Human Histamine A pKi 8.04 8.06 8.09 Drug Central
H4 HRH4 Human Histamine A pKi 8.18 8.18 8.18 Drug Central
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 8.22 8.22 8.22 Drug Central
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 8.23 8.23 8.23 Drug Central
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 8.19 8.19 8.19 Drug Central
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 8.2 8.2 8.2 Drug Central
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 8.18 8.18 8.18 Drug Central
M5 ACM5 Human Acetylcholine (muscarinic) A pKi 8.21 8.21 8.21 Drug Central
α1D ADA1D Human Adrenoceptors A pKi 8.32 8.32 8.32 Drug Central
α2A ADA2A Human Adrenoceptors A pKi 8.29 8.29 8.29 Drug Central
α2B ADA2B Human Adrenoceptors A pKi 8.25 8.25 8.25 Drug Central
H2 HRH2 Human Histamine A pKi 8.29 8.29 8.29 Drug Central
H2 HRH2 Human Histamine A pKi 5.08 5.08 5.08 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 8.25 8.25 8.25 Drug Central
α1B ADA1B Rat Adrenoceptors A pKi 8.3 8.3 8.3 Drug Central
5-HT2C 5HT2C Rat 5-Hydroxytryptamine A pKi 5.51 5.51 5.51 PDSP Ki database
H1 HRH1 Rat Histamine A pKi 8.26 8.41 8.7 ChEMBL
H1 HRH1 Rat Histamine A pKi 8.06 8.06 8.06 Drug Central
5-HT2C 5HT2C Mouse 5-Hydroxytryptamine A pKi 5.3 5.3 5.3 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α1B ADA1B Rat Adrenoceptors A pIC50 4.81 4.81 4.81 ChEMBL
α1D ADA1D Human Adrenoceptors A pIC50 4.47 4.47 4.47 ChEMBL
α2B ADA2B Human Adrenoceptors A pIC50 5.34 5.34 5.34 ChEMBL
M5 ACM5 Human Acetylcholine (muscarinic) A pIC50 5.98 5.98 5.98 ChEMBL
M4 ACM4 Human Acetylcholine (muscarinic) A pIC50 5.7 5.7 5.7 ChEMBL
H1 HRH1 Human Histamine A pIC50 7.18 7.69 8.2 ChEMBL
M3 ACM3 Human Acetylcholine (muscarinic) A pIC50 5.59 5.59 5.59 ChEMBL
α2A ADA2A Human Adrenoceptors A pIC50 4.69 4.69 4.69 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pIC50 5.16 5.16 5.16 ChEMBL
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pIC50 5.63 5.63 5.63 ChEMBL
M1 ACM1 Human Acetylcholine (muscarinic) A pIC50 5.86 5.86 5.86 ChEMBL
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pIC50 5.43 5.43 5.43 ChEMBL
H1 HRH1 Guinea pig Histamine A pIC50 8.09 8.09 8.09 Drug Central
H2 HRH2 Human Histamine A pIC50 5.08 5.08 5.08 ChEMBL
NPS NPSR1 Human Neuropeptide S A Potency 4.9 4.9 4.9 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 4.6 5.05 5.5 ChEMBL
H1 HRH1 Guinea pig Histamine A pIC50 7.92 7.99 8.06 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.9 5.31 5.9 ChEMBL