BDBM50413019 CHEMBL495937

SMILES: CC(C)CCNc1nccc2[nH]c3ccccc3c12

InChI Key: InChIKey=GQDYLWRPYFOLCP-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50413019   

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))	BDBM50413019 (CHEMBL495937) Show SMILES CC(C)CCNc1nccc2[nH]c3ccccc3c12 Show InChI InChI=1S/C16H19N3/c1-11(2)7-9-17-16-15-12-5-3-4-6-13(12)19-14(15)8-10-18-16/h3-6,8,10-11,19H,7,9H2,1-2H3,(H,17,18)	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	12.6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Displacement of [125I]human urotensin 2 from human recombinant urotensin 2 receptor expressed in HEK293 cells				Bioorg Med Chem Lett 18: 4936-9 (2008) Article DOI: 10.1016/j.bmcl.2008.08.054 BindingDB Entry DOI: 10.7270/Q2GH9K5T
					More data for this Ligand-Target Pair
Urotensin II receptor (Felis catus)	BDBM50413019 (CHEMBL495937) Show SMILES CC(C)CCNc1nccc2[nH]c3ccccc3c12 Show InChI InChI=1S/C16H19N3/c1-11(2)7-9-17-16-15-12-5-3-4-6-13(12)19-14(15)8-10-18-16/h3-6,8,10-11,19H,7,9H2,1-2H3,(H,17,18)	KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.58E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Displacement of [125I]human urotensin 2 from cat urotensin 2 receptor expressed in HEK293 cells				Bioorg Med Chem Lett 18: 4936-9 (2008) Article DOI: 10.1016/j.bmcl.2008.08.054 BindingDB Entry DOI: 10.7270/Q2GH9K5T
					More data for this Ligand-Target Pair