null

SMILES: COc1ccc(Cn2c(nc3ccccc23)C2CCCN(C2)C2CCCCC2)cc1

InChI Key: InChIKey=YLEDBIZRBVHBJQ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50316928   

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
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50316928 (2-(1-cyclohexylpiperidin-3-yl)-1-(4-methoxybenzyl)...) Show SMILES COc1ccc(Cn2c(nc3ccccc23)C2CCCN(C2)C2CCCCC2)cc1 Show InChI InChI=1S/C26H33N3O/c1-30-23-15-13-20(14-16-23)18-29-25-12-6-5-11-24(25)27-26(29)21-8-7-17-28(19-21)22-9-3-2-4-10-22/h5-6,11-16,21-22H,2-4,7-10,17-19H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.84E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neurocrine Biosciences Curated by ChEMBL					Assay Description Displacement of [3H]dofetolide from human ERG channel expressed in HEK293 cells by liquid scintillation counting				Bioorg Med Chem Lett 20: 2916-9 (2010) Article DOI: 10.1016/j.bmcl.2010.03.027 BindingDB Entry DOI: 10.7270/Q20865G0
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50316928 (2-(1-cyclohexylpiperidin-3-yl)-1-(4-methoxybenzyl)...) Show SMILES COc1ccc(Cn2c(nc3ccccc23)C2CCCN(C2)C2CCCCC2)cc1 Show InChI InChI=1S/C26H33N3O/c1-30-23-15-13-20(14-16-23)18-29-25-12-6-5-11-24(25)27-26(29)21-8-7-17-28(19-21)22-9-3-2-4-10-22/h5-6,11-16,21-22H,2-4,7-10,17-19H2,1H3	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	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Neurocrine Biosciences Curated by ChEMBL					Assay Description Inhibition of CYP3A4				Bioorg Med Chem Lett 20: 2916-9 (2010) Article DOI: 10.1016/j.bmcl.2010.03.027 BindingDB Entry DOI: 10.7270/Q20865G0
					More data for this Ligand-Target Pair