Molecule Details
InChIKeyDELIRGNMBCRVBU-AJBCFYQKSA-N
Compound NameH-Nal-cyclo[DCys-Pal-DTrp-Lys-Nle-Cys]-Nal-NH2
Canonical SMILESCC(C)CC[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2cccnc2)NC(=O)[C@@H](NC(=O)[C@@H](N)Cc2ccc3ccccc3c2)CSSC[C@@H](C(=O)N[C@@H](Cc2ccc3ccccc3c2)C(N)=O)NC1=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)5
Pfam Stratification Homologous
Avg pChEMBL6.47
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (5)
Target Gene Organism Category Pfam pChEMBL Type Source
P30874 SSTR2 Homo sapiens Human PF00001 7.1 Ki ChEMBL;BindingDB
P32745 SSTR3 Homo sapiens Human PF00001 6.9 Ki ChEMBL;BindingDB
P31391 SSTR4 Homo sapiens Human PF00001 6.2 Ki ChEMBL;BindingDB
P35346 SSTR5 Homo sapiens Human PF00001 6.1 Ki ChEMBL;BindingDB
P30872 SSTR1 Homo sapiens Human PF00001 6.1 Ki ChEMBL;BindingDB