Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50183049   

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))	BDBM50183049 (CHEMBL3819593) Show SMILES [#6]-c1ccc(-[#7]-2-[#6]-[#6]-[#7](-[#6]-[#6]-2)-c2ccc(\[#6]=[#6]-3\[#6](=O)-c4ccccc4-[#6]-3=O)cc2)c(-[#6])c1 Show InChI InChI=1S/C28H26N2O2/c1-19-7-12-26(20(2)17-19)30-15-13-29(14-16-30)22-10-8-21(9-11-22)18-25-27(31)23-5-3-4-6-24(23)28(25)32/h3-12,17-18H,13-16H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	298	n/a	n/a	n/a	n/a	n/a	n/a
University of Delhi Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 2 m...				Bioorg Med Chem 24: 3829-41 (2016) Article DOI: 10.1016/j.bmc.2016.06.027 BindingDB Entry DOI: 10.7270/Q24Q7WXM
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50183049 (CHEMBL3819593) Show SMILES [#6]-c1ccc(-[#7]-2-[#6]-[#6]-[#7](-[#6]-[#6]-2)-c2ccc(\[#6]=[#6]-3\[#6](=O)-c4ccccc4-[#6]-3=O)cc2)c(-[#6])c1 Show InChI InChI=1S/C28H26N2O2/c1-19-7-12-26(20(2)17-19)30-15-13-29(14-16-30)22-10-8-21(9-11-22)18-25-27(31)23-5-3-4-6-24(23)28(25)32/h3-12,17-18H,13-16H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	415	n/a	n/a	n/a	n/a	n/a	n/a
University of Delhi Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 2...				Bioorg Med Chem 24: 3829-41 (2016) Article DOI: 10.1016/j.bmc.2016.06.027 BindingDB Entry DOI: 10.7270/Q24Q7WXM
					More data for this Ligand-Target Pair