Compile Data Set for Download or QSAR

Found 2 hits of ki for monomerid = 50271518   

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 (Homo sapiens (Human))	BDBM50271518 (1,3-bis{[(1,2,3,4-Tetrahydroacridin-9-yl)amino]eth...) Show SMILES Cc1cc(CCNc2c3CCCCc3nc3ccccc23)cc(CCNc2c3CCCCc3nc3ccccc23)c1 Show InChI InChI=1S/C37H40N4/c1-25-22-26(18-20-38-36-28-10-2-6-14-32(28)40-33-15-7-3-11-29(33)36)24-27(23-25)19-21-39-37-30-12-4-8-16-34(30)41-35-17-9-5-13-31(35)37/h2,4,6,8,10,12,14,16,22-24H,3,5,7,9,11,13,15,17-21H2,1H3,(H,38,40)(H,39,41)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.04	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ di Siena Curated by ChEMBL					Assay Description Inhibition of human recombinant BuChE				J Med Chem 51: 3154-70 (2008) Article DOI: 10.1021/jm701253t BindingDB Entry DOI: 10.7270/Q22Z16D4
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50271518 (1,3-bis{[(1,2,3,4-Tetrahydroacridin-9-yl)amino]eth...) Show SMILES Cc1cc(CCNc2c3CCCCc3nc3ccccc23)cc(CCNc2c3CCCCc3nc3ccccc23)c1 Show InChI InChI=1S/C37H40N4/c1-25-22-26(18-20-38-36-28-10-2-6-14-32(28)40-33-15-7-3-11-29(33)36)24-27(23-25)19-21-39-37-30-12-4-8-16-34(30)41-35-17-9-5-13-31(35)37/h2,4,6,8,10,12,14,16,22-24H,3,5,7,9,11,13,15,17-21H2,1H3,(H,38,40)(H,39,41)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.45	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ di Siena Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE				J Med Chem 51: 3154-70 (2008) Article DOI: 10.1021/jm701253t BindingDB Entry DOI: 10.7270/Q22Z16D4
					More data for this Ligand-Target Pair