Molecule Details
InChIKeyRBZTXCPXQHRLIB-COPXCHQZSA-N
Compound NameCyclo Ac-Cys-Glu-His-D-(2'')Nal-Arg-Trp-Gly-Cys-Pro-Pro-Lys-Asp-NH2
Canonical SMILESCC(=O)N[C@@H]1CSSC[C@@H](C(=O)N2CCC[C@H]2C(=O)N2CCC[C@H]2C(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CC(=O)O)NC(=O)CNC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)[C@@H](CCC(=O)O)NC1=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL8.07
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P32245 MC4R Homo sapiens Human PF00001 8.8 Ki ChEMBL;BindingDB
P33032 MC5R Homo sapiens Human PF00001 7.8 Ki ChEMBL;BindingDB
P41968 MC3R Homo sapiens Human PF00001 7.6 Ki ChEMBL;BindingDB