Molecule Details
InChIKeyJNMPZUZCPFIJGJ-MRZQVYDSSA-N
Compound NameH-cyclo[DCys-Phe-Phe-DTrp-Lys-Thr-Phe-DCys]-NH2
Canonical SMILESCC(O)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](N)CSSC[C@H](C(N)=O)NC(=O)[C@H](Cc2ccccc2)NC1=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)5
Pfam Stratification Homologous
Avg pChEMBL8.0
SourceBindingDB
2D Structure
2D structure
Activity Profile
Target Activities (5)
Target Gene Organism Category Pfam pChEMBL Type Source
P35346 SSTR5 Homo sapiens Human PF00001 9.4 Ki BindingDB
P30874 SSTR2 Homo sapiens Human PF00001 7.8 Ki BindingDB
P31391 SSTR4 Homo sapiens Human PF00001 7.8 Ki BindingDB
P30872 SSTR1 Homo sapiens Human PF00001 7.7 Ki BindingDB
P32745 SSTR3 Homo sapiens Human PF00001 7.2 Ki BindingDB