CHEMBL2371978


SMILES CC(C)C[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1cc(C(F)(F)F)cc(C(F)(F)F)c1
InChIKey KNNCZVVJJSCZNH-WPIMGRBNSA-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
μ OPRM Rat Opioid A pKi 6.42 6.42 6.42 ChEMBL
NK1 NK1R Human Tachykinin A pKi 8.52 8.52 8.52 ChEMBL
δ OPRD Human Opioid A pKi 7.03 7.03 7.03 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
δ OPRD Mouse Opioid A pIC50 6.39 6.39 6.39 ChEMBL
μ OPRM Rat Opioid A pIC50 6.09 6.09 6.09 ChEMBL
μ OPRM Rat Opioid A pEC50 6.46 6.46 6.46 ChEMBL
NK1 NK1R Human Tachykinin A pIC50 8.0 8.0 8.0 ChEMBL
δ OPRD Human Opioid A pIC50 6.7 6.7 6.7 ChEMBL
δ OPRD Human Opioid A pEC50 7.77 7.78 7.78 ChEMBL