Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Acetylcholinesterase' and Ligand = 'BDBM50251187'   

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 (Electrophorus electricus (Electric eel))	BDBM50251187 (1-(4-(O-beta-D-Glucopyranosyl) benzylidene) methox...) Show SMILES CO\N=C/c1ccc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1 |r| Show InChI InChI=1S/C14H19NO7/c1-20-15-6-8-2-4-9(5-3-8)21-14-13(19)12(18)11(17)10(7-16)22-14/h2-6,10-14,16-19H,7H2,1H3/b15-6-/t10-,11-,12+,13-,14-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	130	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE by Ellman's method				Eur J Med Chem 43: 166-73 (2008) Article DOI: 10.1016/j.ejmech.2007.03.018 BindingDB Entry DOI: 10.7270/Q2DF6S3Z
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50251187 (1-(4-(O-beta-D-Glucopyranosyl) benzylidene) methox...) Show SMILES CO\N=C/c1ccc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1 |r| Show InChI InChI=1S/C14H19NO7/c1-20-15-6-8-2-4-9(5-3-8)21-14-13(19)12(18)11(17)10(7-16)22-14/h2-6,10-14,16-19H,7H2,1H3/b15-6-/t10-,11-,12+,13-,14-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	490	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE by Ellman's method				Eur J Med Chem 43: 166-73 (2008) Article DOI: 10.1016/j.ejmech.2007.03.018 BindingDB Entry DOI: 10.7270/Q2DF6S3Z
					More data for this Ligand-Target Pair