H-Phe(4-I)-Cys(1)-3Pal-D-Trp-Lys-D-Val-D-Cys(1)-Phe(4-I)-NH2

InChIKey	`IEZYVOCMWNRGPA-HGYOODBQSA-N`
Compound Name	H-Phe(4-I)-Cys(1)-3Pal-D-Trp-Lys-D-Val-D-Cys(1)-Phe(4-I)-NH2
Canonical SMILES	`CC(C)[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)Cc2ccc(I)cc2)CSSC[C@H](C(=O)N[C@@H](Cc2ccc(I)cc2)C(N)=O)NC1=O`
Clinical Status	Data-mined Candidate
Targets (Human+Pathogen)	5
Pfam Stratification	Homologous
Avg pChEMBL	7.03
Source	ChEMBL;BindingDB

2D Structure

Activity Profile

Target	Gene	Organism	Category	Pfam	pChEMBL	Type	Source
P32745	SSTR3	Homo sapiens	Human	PF00001	7.7	Ki	ChEMBL;BindingDB
P30874	SSTR2	Homo sapiens	Human	PF00001	7.5	Ki	ChEMBL;BindingDB
P35346	SSTR5	Homo sapiens	Human	PF00001	7.3	Ki	ChEMBL;BindingDB
P31391	SSTR4	Homo sapiens	Human	PF00001	6.4	Ki	ChEMBL;BindingDB
P30872	SSTR1	Homo sapiens	Human	PF00001	6.2	Ki	ChEMBL;BindingDB