H-D-Phe-D-Cys(1)-Phe-Trp-Lys-Thr-N(Me)Cys(1)-Thr-NH2

InChIKey	`XFGSVYLLRWBKDX-JBJZNJHGSA-N`
Compound Name	H-D-Phe-D-Cys(1)-Phe-Trp-Lys-Thr-N(Me)Cys(1)-Thr-NH2
Canonical SMILES	`C[C@@H](O)[C@H](NC(=O)[C@@H]1CSSC[C@@H](NC(=O)[C@H](N)Cc2ccccc2)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1C)C(N)=O`
Clinical Status	Data-mined Candidate
Targets (Human+Pathogen)	5
Pfam Stratification	Homologous
Avg pChEMBL	6.92
Source	ChEMBL;BindingDB

2D Structure

Activity Profile

Target	Gene	Organism	Category	Pfam	pChEMBL	Type	Source
P35346	SSTR5	Homo sapiens	Human	PF00001	7.5	Kd	ChEMBL;BindingDB
P32745	SSTR3	Homo sapiens	Human	PF00001	7.3	Kd	ChEMBL;BindingDB
P30874	SSTR2	Homo sapiens	Human	PF00001	7.2	Kd	ChEMBL;BindingDB
P31391	SSTR4	Homo sapiens	Human	PF00001	6.2	Kd	ChEMBL;BindingDB
P30872	SSTR1	Homo sapiens	Human	PF00001	6.2	Kd	ChEMBL;BindingDB