BDBM50252310 (R)-N-(1-(3-bromo-4-(piperidin-4-yloxy)phenylsulfonyl)pyrrolidin-3-yl)-3,4-dichlorobenzamide::CHEMBL481964

SMILES: Clc1ccc(cc1Cl)C(=O)N[C@@H]1CCN(C1)S(=O)(=O)c1ccc(OC2CCNCC2)c(Br)c1

InChI Key: InChIKey=KYAZIJKMIRPNBJ-OAHLLOKOSA-N

Data: 1 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 1 hit for monomerid = 50252310   

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 II receptor (Homo sapiens (Human))	BDBM50252310 ((R)-N-(1-(3-bromo-4-(piperidin-4-yloxy)phenylsulfo...) Show SMILES Clc1ccc(cc1Cl)C(=O)N[C@@H]1CCN(C1)S(=O)(=O)c1ccc(OC2CCNCC2)c(Br)c1 |r| Show InChI InChI=1S/C22H24BrCl2N3O4S/c23-18-12-17(2-4-21(18)32-16-5-8-26-9-6-16)33(30,31)28-10-7-15(13-28)27-22(29)14-1-3-19(24)20(25)11-14/h1-4,11-12,15-16,26H,5-10,13H2,(H,27,29)/t15-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	380	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Antagonist activity at human recombinant urotensin 2 receptor expressed in HEK293 cells assessed as inhibition of urotensin 2-induced calcium mobiliz...				Bioorg Med Chem Lett 18: 3950-4 (2008) Article DOI: 10.1016/j.bmcl.2008.06.019 BindingDB Entry DOI: 10.7270/Q2FT8KTR
					More data for this Ligand-Target Pair