Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Acetylcholinesterase' and Ligand = 'BDBM50114366'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Acetylcholinesterase (Homo sapiens (Human))	BDBM50114366 (CHEMBL3604197) Show SMILES Cl.CN(C)c1ccc(cc1)C(=O)NCCCCCCCNc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C29H38N4O.ClH/c1-33(2)23-18-16-22(17-19-23)29(34)31-21-11-5-3-4-10-20-30-28-24-12-6-8-14-26(24)32-27-15-9-7-13-25(27)28;/h6,8,12,14,16-19H,3-5,7,9-11,13,15,20-21H2,1-2H3,(H,30,32)(H,31,34);1H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	75	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of acetylcholinesterase in human erythrocytes using acetylthiocholine iodide substrate by spectrophotometric Ellman's method				Bioorg Med Chem 23: 5610-8 (2015) Article DOI: 10.1016/j.bmc.2015.07.029 BindingDB Entry DOI: 10.7270/Q25T3N9G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50114366 (CHEMBL3604197) Show SMILES Cl.CN(C)c1ccc(cc1)C(=O)NCCCCCCCNc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C29H38N4O.ClH/c1-33(2)23-18-16-22(17-19-23)29(34)31-21-11-5-3-4-10-20-30-28-24-12-6-8-14-26(24)32-27-15-9-7-13-25(27)28;/h6,8,12,14,16-19H,3-5,7,9-11,13,15,20-21H2,1-2H3,(H,30,32)(H,31,34);1H	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	167	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using ATC iodide substrate by Ellman's assay				Bioorg Med Chem 23: 5610-8 (2015) Article DOI: 10.1016/j.bmc.2015.07.029 BindingDB Entry DOI: 10.7270/Q25T3N9G
					More data for this Ligand-Target Pair