Molecule Details
InChIKeyLMTCYYTZYVZVDJ-WCHRTOSNSA-N
Compound NameAc-Gly-Ser-Gln-His-Ser-Nle-Glu(1)-Hyp-D-Phe-Arg-Trp-Lys(1)-NH2
Canonical SMILESCCCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)CNC(C)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(N)=O)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H]2C[C@@H](O)CN2C1=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)4
Pfam Stratification Homologous
Avg pChEMBL7.67
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (4)
Target Gene Organism Category Pfam pChEMBL Type Source
P32245 MC4R Homo sapiens Human PF00001 8.3 Ki ChEMBL;BindingDB
P33032 MC5R Homo sapiens Human PF00001 8.3 Ki ChEMBL;BindingDB
P41968 MC3R Homo sapiens Human PF00001 7.3 Ki ChEMBL;BindingDB
Q01726 MC1R Homo sapiens Human PF00001 6.7 Ki ChEMBL;BindingDB