BDBM50251944 (R)-N-(1-(4-(3-(dimethylamino)propoxy)benzyl)pyrrolidin-3-yl)-4-bromobenzamide::CHEMBL480170

SMILES: CN(C)CCCOc1ccc(CN2CC[C@H](C2)NC(=O)c2ccc(Br)cc2)cc1

InChI Key: InChIKey=FBJCHFHVYRMSBS-OAQYLSRUSA-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 = 50251944   

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))	BDBM50251944 ((R)-N-(1-(4-(3-(dimethylamino)propoxy)benzyl)pyrro...) Show SMILES CN(C)CCCOc1ccc(CN2CC[C@H](C2)NC(=O)c2ccc(Br)cc2)cc1 |r| Show InChI InChI=1S/C23H30BrN3O2/c1-26(2)13-3-15-29-22-10-4-18(5-11-22)16-27-14-12-21(17-27)25-23(28)19-6-8-20(24)9-7-19/h4-11,21H,3,12-17H2,1-2H3,(H,25,28)/t21-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	350	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