zacopride


SMILES COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl
InChIKey FEROPKNOYKURCJ-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 2
Rotatable bonds 3
Molecular weight (Da) 309.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Ligand site mutations 5-HT4

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT4 5HT4R Human 5-Hydroxytryptamine A pKi 4.9 5.75 6.6 Guide to Pharmacology
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pKi 5.9 6.4 6.9 Guide to Pharmacology
5-HT4 5HT4R Mouse 5-Hydroxytryptamine A pKi 6.7 6.7 6.7 Guide to Pharmacology
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pKi 6.12 6.46 6.8 ChEMBL
5-HT5A 5HT5A Human 5-Hydroxytryptamine A pKi 4.8 4.8 4.8 ChEMBL
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pKi 5.9 6.34 7.0 PDSP Ki database
5-HT4 5HT4R Mouse 5-Hydroxytryptamine A pKi 5.97 6.5 6.72 PDSP Ki database
5-HT1B 5HT1B Human 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
5-HT1D 5HT1D Human 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
5-HT2A 5HT2A Rat 5-Hydroxytryptamine A pKi 6.15 6.15 6.15 PDSP Ki database
5-HT2C 5HT2C Rat 5-Hydroxytryptamine A pKi 5.47 5.47 5.47 PDSP Ki database
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 5.87 5.87 5.87 PDSP Ki database
5-HT2B 5HT2B Human 5-Hydroxytryptamine A pKi 6.29 6.29 6.29 PDSP Ki database
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 6.1 6.1 6.1 PDSP Ki database
5-HT5A 5HT5A Rat 5-Hydroxytryptamine A pKi 6.0 6.0 6.0 PDSP Ki database
5-HT7 5HT7R Rat 5-Hydroxytryptamine A pKi 6.0 6.05 6.26 PDSP Ki database
5-HT4 5HT4R Human 5-Hydroxytryptamine A pKi 6.55 6.55 6.55 PDSP Ki database
5-HT7 5HT7R Human 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
5-HT1E 5HT1E Human 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
5-HT1F 5HT1F Human 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database