BDBM84645 L-363,376::cyclo(Pro-Ala-Trp-Lys-Thr-Phe)

SMILES: C[C@@H](O)[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC1=O

InChI Key: InChIKey=PHCCTJXHGSJHSO-UHFFFAOYSA-N

Data: 3 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 84645   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Somatostatin receptor type 3 (Mouse)	BDBM84645 (cyclo(Pro-Ala-Trp-Lys-Thr-Phe) | L-363,376) Show SMILES Show InChI	GoogleScholar	UniChem		244	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Somatostatin receptor type 2 (Mouse)	BDBM84645 (cyclo(Pro-Ala-Trp-Lys-Thr-Phe) | L-363,376) Show SMILES Show InChI	GoogleScholar	UniChem		356	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Somatostatin receptor type 1 (Human)	BDBM84645 (cyclo(Pro-Ala-Trp-Lys-Thr-Phe) | L-363,376) Show SMILES Show InChI	GoogleScholar	UniChem		1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair