BDBM50414765 CHEMBL578654

SMILES: COc1ccc(cc1)-c1ccc(cc1)C(=O)NC(CCN(C)C)c1ccc2ccccc2c1

InChI Key: InChIKey=FGUKIDJCMKJULI-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 = 50414765   

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))	BDBM50414765 (CHEMBL578654) Show SMILES COc1ccc(cc1)-c1ccc(cc1)C(=O)NC(CCN(C)C)c1ccc2ccccc2c1 Show InChI InChI=1S/C29H30N2O2/c1-31(2)19-18-28(26-13-10-21-6-4-5-7-25(21)20-26)30-29(32)24-11-8-22(9-12-24)23-14-16-27(33-3)17-15-23/h4-17,20,28H,18-19H2,1-3H3,(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	105	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