null

SMILES: C(C1CCCCN1)N1CCN(C1)c1ccccc1

InChI Key: InChIKey=HVBAGGJDXDXSAY-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50313619   

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
Histamine H1 receptor (Homo sapiens (Human))	BDBM50313619 (2-((3-phenylimidazolidin-1-yl)methyl)piperidine | ...) Show SMILES C(C1CCCCN1)N1CCN(C1)c1ccccc1 Show InChI InChI=1S/C15H23N3/c1-2-7-15(8-3-1)18-11-10-17(13-18)12-14-6-4-5-9-16-14/h1-3,7-8,14,16H,4-6,9-13H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.51E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Activity at histamine H1 receptor				Bioorg Med Chem Lett 20: 2013-6 (2010) Article DOI: 10.1016/j.bmcl.2010.01.090 BindingDB Entry DOI: 10.7270/Q27P8ZJG
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50313619 (2-((3-phenylimidazolidin-1-yl)methyl)piperidine | ...) Show SMILES C(C1CCCCN1)N1CCN(C1)c1ccccc1 Show InChI InChI=1S/C15H23N3/c1-2-7-15(8-3-1)18-11-10-17(13-18)12-14-6-4-5-9-16-14/h1-3,7-8,14,16H,4-6,9-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.58E+4	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Displacement of [3H]dofetilide from human ERG by scintillation proximity assay				Bioorg Med Chem Lett 20: 2013-6 (2010) Article DOI: 10.1016/j.bmcl.2010.01.090 BindingDB Entry DOI: 10.7270/Q27P8ZJG
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50313619 (2-((3-phenylimidazolidin-1-yl)methyl)piperidine | ...) Show SMILES C(C1CCCCN1)N1CCN(C1)c1ccccc1 Show InChI InChI=1S/C15H23N3/c1-2-7-15(8-3-1)18-11-10-17(13-18)12-14-6-4-5-9-16-14/h1-3,7-8,14,16H,4-6,9-13H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Inhibition of human recombinant CYP2D6 by spectrafluorometry				Bioorg Med Chem Lett 20: 2013-6 (2010) Article DOI: 10.1016/j.bmcl.2010.01.090 BindingDB Entry DOI: 10.7270/Q27P8ZJG
					More data for this Ligand-Target Pair