Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Cholinesterase' and Ligand = 'BDBM50204837'   

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
Cholinesterase (Equus caballus (Horse))	BDBM50204837 (CHEMBL3900401) Show SMILES COc1cc2CC(CC3CCN(Cc4ncc(C)cc4C)CC3)C(=O)c2cc1OC Show InChI InChI=1S/C25H32N2O3/c1-16-9-17(2)22(26-14-16)15-27-7-5-18(6-8-27)10-20-11-19-12-23(29-3)24(30-4)13-21(19)25(20)28/h9,12-14,18,20H,5-8,10-11,15H2,1-4H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.31E+3	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using s-butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured up to...				Eur J Med Chem 123: 282-297 (2016) Article DOI: 10.1016/j.ejmech.2016.07.052 BindingDB Entry DOI: 10.7270/Q2ZW1NW5
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50204837 (CHEMBL3900401) Show SMILES COc1cc2CC(CC3CCN(Cc4ncc(C)cc4C)CC3)C(=O)c2cc1OC Show InChI InChI=1S/C25H32N2O3/c1-16-9-17(2)22(26-14-16)15-27-7-5-18(6-8-27)10-20-11-19-12-23(29-3)24(30-4)13-21(19)25(20)28/h9,12-14,18,20H,5-8,10-11,15H2,1-4H3	PDB MMDB 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	8.55E+3	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using s-butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured up to ...				Eur J Med Chem 123: 282-297 (2016) Article DOI: 10.1016/j.ejmech.2016.07.052 BindingDB Entry DOI: 10.7270/Q2ZW1NW5
					More data for this Ligand-Target Pair