BDBM50414783 CHEMBL573575

SMILES: CN(C)CCC(NC(=O)c1cccc(c1)-c1ccc2ccccc2c1)c1ccc(Cl)cc1

InChI Key: InChIKey=JBMJUKFNCFTHQA-UHFFFAOYSA-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 = 50414783   

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))	BDBM50414783 (CHEMBL573575) Show SMILES CN(C)CCC(NC(=O)c1cccc(c1)-c1ccc2ccccc2c1)c1ccc(Cl)cc1 Show InChI InChI=1S/C28H27ClN2O/c1-31(2)17-16-27(21-12-14-26(29)15-13-21)30-28(32)25-9-5-8-23(19-25)24-11-10-20-6-3-4-7-22(20)18-24/h3-15,18-19,27H,16-17H2,1-2H3,(H,30,32)	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	363	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