CHEMBL205306


SMILES CCCC[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)CNC(=O)[C@@H](CCCC)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O
InChIKey YVOYRMXNVINXII-PREDZLEHSA-N

Chemical properties

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

Drug properties

Molecular type Protein
Physiological/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 5.66 5.66 5.66 ChEMBL
μ OPRM Rat Opioid A pKi 6.57 6.57 6.57 ChEMBL
δ OPRD Human Opioid A pKi 7.7 7.7 7.7 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
δ OPRD Mouse Opioid A pIC50 6.51 6.51 6.51 ChEMBL
CCK2 GASR Human Cholecystokinin A pIC50 5.66 5.66 5.66 ChEMBL
μ OPRM Rat Opioid A pIC50 6.2 6.2 6.2 ChEMBL
μ OPRM Rat Opioid A pEC50 7.7 7.7 7.7 ChEMBL
δ OPRD Human Opioid A pIC50 7.32 7.32 7.32 ChEMBL
δ OPRD Human Opioid A pEC50 8.39 8.39 8.39 ChEMBL