null

SMILES: COc1cccc(c1)-c1c(cc2ccccn12)C(=O)N1CCCCC1CO

InChI Key: InChIKey=CORFFCKGBFFQAQ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50395947   

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))	BDBM50395947 (CHEMBL2164886) Show SMILES COc1cccc(c1)-c1c(cc2ccccn12)C(=O)N1CCCCC1CO Show InChI InChI=1S/C22H24N2O3/c1-27-19-10-6-7-16(13-19)21-20(14-17-8-2-4-11-23(17)21)22(26)24-12-5-3-9-18(24)15-25/h2,4,6-8,10-11,13-14,18,25H,3,5,9,12,15H2,1H3	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	501	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))	BDBM50395947 (CHEMBL2164886) Show SMILES COc1cccc(c1)-c1c(cc2ccccn12)C(=O)N1CCCCC1CO Show InChI InChI=1S/C22H24N2O3/c1-27-19-10-6-7-16(13-19)21-20(14-17-8-2-4-11-23(17)21)22(26)24-12-5-3-9-18(24)15-25/h2,4,6-8,10-11,13-14,18,25H,3,5,9,12,15H2,1H3	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	>3.31E+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