CHEMBL205965


SMILES CCCC[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O)N(C)C(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CNC(=O)[C@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1
InChIKey XMLJSDGQSNTHPG-TVUSJDTQSA-N

Chemical properties

Hydrogen bond acceptors None
Hydrogen bond donors None
Rotatable bonds None
Molecular weight (Da)

Drug properties

Molecular type Protein
Endogenous/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
CCK2 GASR Human Cholecystokinin A pKi 8.57 8.57 8.57 ChEMBL
μ OPRM Rat Opioid A pKi 5.58 5.58 5.58 ChEMBL
δ OPRD Human Opioid A pKi 7.07 7.07 7.07 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
CCK2 GASR Human Cholecystokinin A pEC50 7.44 7.44 7.44 ChEMBL
CCK2 GASR Human Cholecystokinin A pIC50 8.57 8.57 8.57 ChEMBL
δ OPRD Mouse Opioid A pIC50 6.05 6.05 6.05 ChEMBL
CCK1 CCKAR Human Cholecystokinin A pIC50 4.98 4.98 4.98 ChEMBL
μ OPRM Rat Opioid A pEC50 6.05 6.05 6.05 ChEMBL
μ OPRM Rat Opioid A pIC50 5.22 5.22 5.22 ChEMBL
δ OPRD Human Opioid A pEC50 6.05 6.05 6.05 ChEMBL
δ OPRD Human Opioid A pIC50 6.7 6.7 6.7 ChEMBL