Molecule Details
InChIKeyQIXXUKXLULSIND-TTZRXDBLSA-N
Compound NameH-Ala-Gly-Cys(1)-Lys-Asn-Phe-Phe-D-Tyr-Lys-Thr-Phe-Thr-Ser-Cys(1)-OH
Canonical SMILESC[C@H](N)C(=O)NCC(=O)N[C@H]1CSSC[C@@H](C(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2ccc(O)cc2)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)5
Pfam Stratification Homologous
Avg pChEMBL7.83
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (5)
Target Gene Organism Category Pfam pChEMBL Type Source
P32745 SSTR3 Homo sapiens Human PF00001 8.7 IC50 ChEMBL;BindingDB
P30874 SSTR2 Homo sapiens Human PF00001 8.4 IC50 ChEMBL;BindingDB
P31391 SSTR4 Homo sapiens Human PF00001 7.8 IC50 ChEMBL;BindingDB
P35346 SSTR5 Homo sapiens Human PF00001 7.4 IC50 ChEMBL;BindingDB
P30872 SSTR1 Homo sapiens Human PF00001 6.8 IC50 ChEMBL;BindingDB