Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50317194   

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))	BDBM50317194 (2-[4-(beta-Carboline-2-ium-2-yl)butyl]-beta-carbol...) Show SMILES C(CC[n+]1ccc2c(c1)[nH]c1ccccc21)C[n+]1ccc2c(c1)[nH]c1ccccc21 Show InChI InChI=1S/C26H22N4/c1-3-9-23-19(7-1)21-11-15-29(17-25(21)27-23)13-5-6-14-30-16-12-22-20-8-2-4-10-24(20)28-26(22)18-30/h1-4,7-12,15-18H,5-6,13-14H2/p+2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	78	n/a	n/a	n/a	n/a	n/a	n/a
Friedrich-Schiller-Universitat Jena Curated by ChEMBL					Assay Description Inhibition of equine serum BChE by modified Ellman's method				J Med Chem 53: 3611-7 (2010) Article DOI: 10.1021/jm1000024 BindingDB Entry DOI: 10.7270/Q2SJ1KS0
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50317194 (2-[4-(beta-Carboline-2-ium-2-yl)butyl]-beta-carbol...) Show SMILES C(CC[n+]1ccc2c(c1)[nH]c1ccccc21)C[n+]1ccc2c(c1)[nH]c1ccccc21 Show InChI InChI=1S/C26H22N4/c1-3-9-23-19(7-1)21-11-15-29(17-25(21)27-23)13-5-6-14-30-16-12-22-20-8-2-4-10-24(20)28-26(22)18-30/h1-4,7-12,15-18H,5-6,13-14H2/p+2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	278	n/a	n/a	n/a	n/a	n/a	n/a
Friedrich-Schiller-Universitat Jena Curated by ChEMBL					Assay Description Inhibition of electric eel AChE by modified Ellman's method				J Med Chem 53: 3611-7 (2010) Article DOI: 10.1021/jm1000024 BindingDB Entry DOI: 10.7270/Q2SJ1KS0
					More data for this Ligand-Target Pair