Molecule Details
InChIKeyHAZKRENFRTVGPO-IYHFWKIMSA-N
Compound NameH-Ala-Gly-Cys(1)-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Ala-Ser-Cys(1)-NH2
Canonical SMILESC[C@H](N)C(=O)NCC(=O)N[C@H]1CSSC[C@@H](C(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H]([C@@H](C)O)NC(=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](CC(N)=O)NC(=O)[C@H](CCCCN)NC1=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)4
Pfam Stratification Homologous
Avg pChEMBL9.2
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (4)
Target Gene Organism Category Pfam pChEMBL Type Source
P35346 SSTR5 Homo sapiens Human PF00001 9.4 Ki ChEMBL;BindingDB
P30872 SSTR1 Homo sapiens Human PF00001 9.3 Ki ChEMBL;BindingDB
P32745 SSTR3 Homo sapiens Human PF00001 9.2 Ki ChEMBL;BindingDB
P30874 SSTR2 Homo sapiens Human PF00001 8.9 Ki ChEMBL;BindingDB