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SMILES: OCC1CCCCN1C(=O)c1cc2ccccn2c1-c1cccc(c1)C#N

InChI Key: InChIKey=KZZYOAHUNVIUHK-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50395946   

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
Transient receptor potential cation channel subfamily V member 1 (Homo sapiens (Human))	BDBM50395946 (CHEMBL2164887) Show SMILES OCC1CCCCN1C(=O)c1cc2ccccn2c1-c1cccc(c1)C#N Show InChI InChI=1S/C22H21N3O2/c23-14-16-6-5-7-17(12-16)21-20(13-18-8-1-3-10-24(18)21)22(27)25-11-4-2-9-19(25)15-26/h1,3,5-8,10,12-13,19,26H,2,4,9,11,15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.98E+3	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Antagonist activity at human TRPV1 expressed in CHO cells by IonWorks assay				Bioorg Med Chem Lett 22: 6888-95 (2012) Article DOI: 10.1016/j.bmcl.2012.09.059 BindingDB Entry DOI: 10.7270/Q26W9C63
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50395946 (CHEMBL2164887) Show SMILES OCC1CCCCN1C(=O)c1cc2ccccn2c1-c1cccc(c1)C#N Show InChI InChI=1S/C22H21N3O2/c23-14-16-6-5-7-17(12-16)21-20(13-18-8-1-3-10-24(18)21)22(27)25-11-4-2-9-19(25)15-26/h1,3,5-8,10,12-13,19,26H,2,4,9,11,15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.45E+4	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human ERG expressed in CHO cells by IonWorks assay				Bioorg Med Chem Lett 22: 6888-95 (2012) Article DOI: 10.1016/j.bmcl.2012.09.059 BindingDB Entry DOI: 10.7270/Q26W9C63
					More data for this Ligand-Target Pair