Molecule Details
InChIKeyREMHNXQVRVXAGT-ZYVZXDBOSA-N
Compound NameAc-Nle-c[Asp-trans-4-guanidinyl-Pro-DNal(2'')-Arg-Trp-Lys]-NH2
Canonical SMILESCCCC[C@H](NC(C)=O)C(=O)N[C@H]1CC(=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](Cc2ccc3ccccc3c2)NC(=O)[C@@H]2C[C@@H](NC(=N)N)CN2C1=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)4
Pfam Stratification Homologous
Avg pChEMBL8.81
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (4)
Target Gene Organism Category Pfam pChEMBL Type Source
P33032 MC5R Homo sapiens Human PF00001 9.2 IC50 ChEMBL;BindingDB
P32245 MC4R Homo sapiens Human PF00001 8.8 IC50 ChEMBL;BindingDB
P41968 MC3R Homo sapiens Human PF00001 8.6 IC50 ChEMBL;BindingDB
Q01726 MC1R Homo sapiens Human PF00001 8.6 IC50 ChEMBL;BindingDB