null

SMILES: O=C(CCC1CCN(Cc2ccccc2)CC1)c1ccc2NCCCc2c1

InChI Key: InChIKey=UUQBDBYKPIHDLS-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50318853   

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
Acetylcholinesterase (Homo sapiens (Human))	BDBM50318853 (3-(1-benzylpiperidin-4-yl)-1-(1,2,3,4-tetrahydroqu...) Show SMILES O=C(CCC1CCN(Cc2ccccc2)CC1)c1ccc2NCCCc2c1 Show InChI InChI=1S/C24H30N2O/c27-24(22-9-10-23-21(17-22)7-4-14-25-23)11-8-19-12-15-26(16-13-19)18-20-5-2-1-3-6-20/h1-3,5-6,9-10,17,19,25H,4,7-8,11-16,18H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	54	n/a	n/a	n/a	n/a	n/a	n/a
Sichuan University Curated by ChEMBL					Assay Description Inhibition of AChE				Eur J Med Chem 45: 1167-72 (2010) Article DOI: 10.1016/j.ejmech.2009.12.038 BindingDB Entry DOI: 10.7270/Q25H7GFM
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50318853 (3-(1-benzylpiperidin-4-yl)-1-(1,2,3,4-tetrahydroqu...) Show SMILES O=C(CCC1CCN(Cc2ccccc2)CC1)c1ccc2NCCCc2c1 Show InChI InChI=1S/C24H30N2O/c27-24(22-9-10-23-21(17-22)7-4-14-25-23)11-8-19-12-15-26(16-13-19)18-20-5-2-1-3-6-20/h1-3,5-6,9-10,17,19,25H,4,7-8,11-16,18H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	64.6	n/a	n/a	n/a	n/a	n/a	n/a
Universidade Federal do Rio de Janeiro (UFRJ) Curated by ChEMBL					Assay Description Inhibition of human acetylcholinesterase				Eur J Med Chem 46: 39-51 (2010) Article DOI: 10.1016/j.ejmech.2010.10.009 BindingDB Entry DOI: 10.7270/Q2SX6FG0
					More data for this Ligand-Target Pair