BDBM50011542 3-[4-(carboxymethyl)phenyl]propanoyl-Met-Gly-Trp-Met-Asp-Phe-NH2::CHEMBL273344

SMILES: CSCC[C@H](NC(=O)CCc1ccc(CC(O)=O)cc1)C(=O)NCC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

InChI Key: InChIKey=SIRFEAODYXDUGI-LQWITFIISA-N

Data: 2 IC50

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 2 hits for monomerid = 50011542   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Cholecystokinin receptor (RAT)	BDBM50011542 (3-[4-(carboxymethyl)phenyl]propanoyl-Met-Gly-Trp-M...) Show SMILES CSCC[C@H](NC(=O)CCc1ccc(CC(O)=O)cc1)C(=O)NCC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O Show InChI InChI=1S/C47H58N8O11S2/c1-67-20-18-34(51-39(56)17-16-28-12-14-30(15-13-28)23-41(58)59)44(63)50-27-40(57)52-37(24-31-26-49-33-11-7-6-10-32(31)33)46(65)53-35(19-21-68-2)45(64)55-38(25-42(60)61)47(66)54-36(43(48)62)22-29-8-4-3-5-9-29/h3-15,26,34-38,49H,16-25,27H2,1-2H3,(H2,48,62)(H,50,63)(H,51,56)(H,52,57)(H,53,65)(H,54,66)(H,55,64)(H,58,59)(H,60,61)/t34-,35-,36-,37-,38-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of [3H]-propanoyl binding to cholecystokinin type A receptor was determined in fresh rat pancreatic tissue membranes				J Med Chem 34: 1125-36 (1991) BindingDB Entry DOI: 10.7270/Q27P8XCT
					More data for this Ligand-Target Pair
Cholecystokinin B receptor (Bos taurus)	BDBM50011542 (3-[4-(carboxymethyl)phenyl]propanoyl-Met-Gly-Trp-M...) Show SMILES CSCC[C@H](NC(=O)CCc1ccc(CC(O)=O)cc1)C(=O)NCC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O Show InChI InChI=1S/C47H58N8O11S2/c1-67-20-18-34(51-39(56)17-16-28-12-14-30(15-13-28)23-41(58)59)44(63)50-27-40(57)52-37(24-31-26-49-33-11-7-6-10-32(31)33)46(65)53-35(19-21-68-2)45(64)55-38(25-42(60)61)47(66)54-36(43(48)62)22-29-8-4-3-5-9-29/h3-15,26,34-38,49H,16-25,27H2,1-2H3,(H2,48,62)(H,50,63)(H,51,56)(H,52,57)(H,53,65)(H,54,66)(H,55,64)(H,58,59)(H,60,61)/t34-,35-,36-,37-,38-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
Roche Research Center Curated by ChEMBL					Assay Description Inhibition of [3H]-propanoyl binding to cholecystokinin type B receptor subtype was determined in bovine striatum membranes				J Med Chem 34: 1125-36 (1991) BindingDB Entry DOI: 10.7270/Q27P8XCT
					More data for this Ligand-Target Pair