BDBM50413022 CHEMBL497172

SMILES: CCCCCNc1nccc2[nH]c3ccccc3c12

InChI Key: InChIKey=QIUBQAXHKBRFBV-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 = 50413022   

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))	BDBM50413022 (CHEMBL497172) Show SMILES CCCCCNc1nccc2[nH]c3ccccc3c12 Show InChI InChI=1S/C16H19N3/c1-2-3-6-10-17-16-15-12-7-4-5-8-13(12)19-14(15)9-11-18-16/h4-5,7-9,11,19H,2-3,6,10H2,1H3,(H,17,18)	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.98	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)	BDBM50413022 (CHEMBL497172) Show SMILES CCCCCNc1nccc2[nH]c3ccccc3c12 Show InChI InChI=1S/C16H19N3/c1-2-3-6-10-17-16-15-12-7-4-5-8-13(12)19-14(15)9-11-18-16/h4-5,7-9,11,19H,2-3,6,10H2,1H3,(H,17,18)	KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	398	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