CHEMBL269068


SMILES C[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)C(C)(C)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(N)=O
InChIKey LBZMGFMIRYMDNB-ZJXZEEHCSA-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
NOP OPRX Guinea pig Opioid A pKd 7.33 7.33 7.33 ChEMBL
NOP OPRX Mouse Opioid A pKd 7.46 7.46 7.46 ChEMBL
NOP OPRX Rat Opioid A pKd 7.06 7.06 7.06 ChEMBL
NOP OPRX Human Opioid A pKd 8.68 8.68 8.68 ChEMBL
NOP OPRX Human Opioid A pKi 9.75 9.75 9.75 ChEMBL
κ OPRK Human Opioid A pKi 6.17 6.17 6.17 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database