H-D-Cys(1)-D-Phe-D-Phe-D-Trp-D-Lys-Thr-D-Phe-D-Cys(1)-OH

InChIKey	`PJRZZHKHLDKTKL-GSOBWXQSSA-N`
Compound Name	H-D-Cys(1)-D-Phe-D-Phe-D-Trp-D-Lys-Thr-D-Phe-D-Cys(1)-OH
Canonical SMILES	`C[C@@H](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(=O)O)NC(=O)[C@@H](Cc2ccccc2)NC1=O`
Clinical Status	Data-mined Candidate
Targets (Human+Pathogen)	5
Pfam Stratification	Homologous
Avg pChEMBL	7.79
Source	ChEMBL;BindingDB

2D Structure

Activity Profile

Target	Gene	Organism	Category	Pfam	pChEMBL	Type	Source
P31391	SSTR4	Homo sapiens	Human	PF00001	8.7	IC50	ChEMBL;BindingDB
P32745	SSTR3	Homo sapiens	Human	PF00001	7.9	IC50	ChEMBL;BindingDB
P30872	SSTR1	Homo sapiens	Human	PF00001	7.6	IC50	ChEMBL;BindingDB
P30874	SSTR2	Homo sapiens	Human	PF00001	7.4	IC50	ChEMBL;BindingDB
P35346	SSTR5	Homo sapiens	Human	PF00001	7.3	IC50	ChEMBL;BindingDB