BDBM50414789 CHEMBL573392

SMILES: CN(C)CC[C@H](NC(=O)c1ccc(cc1)-c1ccc(Cl)cc1)c1ccc2ccccc2c1

InChI Key: InChIKey=BWYFLBGAWSTHKC-MHZLTWQESA-N

Data: 1 EC50

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 1 hit for monomerid = 50414789   

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
Urotensin-2 (Homo sapiens (Human))	BDBM50414789 (CHEMBL573392) Show SMILES CN(C)CC[C@H](NC(=O)c1ccc(cc1)-c1ccc(Cl)cc1)c1ccc2ccccc2c1 |r| Show InChI InChI=1S/C28H27ClN2O/c1-31(2)18-17-27(25-12-9-20-5-3-4-6-24(20)19-25)30-28(32)23-10-7-21(8-11-23)22-13-15-26(29)16-14-22/h3-16,19,27H,17-18H2,1-2H3,(H,30,32)/t27-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	22.9	n/a	n/a	n/a	n/a
University of Gothenburg Curated by ChEMBL					Assay Description Agonist activity against human urotensin 2 receptor expressed in human NIH373 cells assessed as beta-galactosidase activity after 5 days by R-SAT ass...				Bioorg Med Chem 17: 4657-65 (2009) Article DOI: 10.1016/j.bmc.2009.04.062 BindingDB Entry DOI: 10.7270/Q20866J9
					More data for this Ligand-Target Pair