Molecule Details
InChIKeyPWVUYOZSIWYFJW-MYBKRMQRSA-N
Compound NameAc-YRC(Me)*EHdFRWC(Me)NH2
Canonical SMILESCSC[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CSC)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(C)=O)C(N)=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)4
Pfam Stratification Homologous
Avg pChEMBL7.61
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (4)
Target Gene Organism Category Pfam pChEMBL Type Source
Q01726 MC1R Homo sapiens Human PF00001 8.6 Ki ChEMBL;BindingDB
P32245 MC4R Homo sapiens Human PF00001 7.9 Ki ChEMBL;BindingDB
P33032 MC5R Homo sapiens Human PF00001 7.2 Ki ChEMBL;BindingDB
P41968 MC3R Homo sapiens Human PF00001 6.8 Ki ChEMBL;BindingDB