CHEMBL1627325


SMILES CSCC[C@H](NC(=O)CNC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](N)CO)C(C)(C)C)C(C)C)[C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)O)[C@@H](C)O
InChIKey WFRTYDJMZVPQJC-JBOYQHEBSA-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

Sankey plot

Compound is not listed as a drug.

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
UT UR2R Human Urotensin A pEC50 8.46 8.46 8.46 ChEMBL
NOP OPRX Human Opioid A pEC50 9.55 9.55 9.55 ChEMBL
NK1 NK1R Human Tachykinin A pEC50 10.31 10.31 10.31 ChEMBL
δ OPRD Human Opioid A pEC50 8.71 8.71 8.71 ChEMBL
κ OPRK Human Opioid A pEC50 8.63 8.63 8.63 ChEMBL
μ OPRM Human Opioid A pEC50 7.96 7.96 7.96 ChEMBL
B2 BKRB2 Human Bradykinin A pEC50 10.47 10.47 10.47 ChEMBL
PAR2 PAR2 Human Proteinase-activated A pEC50 4.5 4.5 4.5 ChEMBL