CLEBOPRIDE


SMILES COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1
InChIKey BVPWJMCABCPUQY-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 2
Rotatable bonds 5
Molecular weight (Da) 373.2

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Ligand site mutations D2

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
D1 DRD1 Bovine Dopamine A pKi 5.22 5.22 5.22 ChEMBL
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pKi 6.98 6.98 6.98 ChEMBL
D2 DRD2 Rat Dopamine A pKi 7.92 8.36 8.95 ChEMBL
D4 DRD4 Human Dopamine A pKi 8.49 8.49 8.49 ChEMBL
D3 DRD3 Human Dopamine A pKi 6.77 7.38 7.98 ChEMBL
D2 DRD2 Human Dopamine A pKi 7.75 7.83 7.92 ChEMBL
5-HT4 5HT4R Mouse 5-Hydroxytryptamine A pKi 7.27 7.27 7.27 PDSP Ki database
D3 DRD3 Rat Dopamine A pKi 7.98 7.98 7.98 PDSP Ki database
D2 DRD2 Mouse Dopamine A pKi 8.89 8.89 8.89 PDSP Ki database
D1 DRD1 Mouse Dopamine A pKi 6.09 6.09 6.09 PDSP Ki database
D2 DRD2 Human Dopamine A pKi 8.1 8.1 8.1 Drug Central
D3 DRD3 Human Dopamine A pKi 8.1 8.1 8.1 Drug Central
D4 DRD4 Human Dopamine A pKi 8.07 8.07 8.07 Drug Central
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pKi 8.16 8.16 8.16 Drug Central
D1 DRD1 Bovine Dopamine A pKi 8.28 8.28 8.28 Drug Central
D2 DRD2 Rat Dopamine A pKi 8.05 8.05 8.05 Drug Central
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
D2 DRD2 Rat Dopamine A pIC50 7.77 7.77 7.77 ChEMBL