null

SMILES: COc1ccc2cc3-c4cc5OCOc5cc4CCn3cc2\c1=[NH+]\CCCc1ccccc1

InChI Key: InChIKey=QVPJDIBOBIFSBR-ZIADKAODSA-O

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50358082   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Cholinesterase (Equus caballus (Horse))	BDBM50358082 (CHEMBL1915196) Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CCn3cc2\c1=[NH+]\CCCc1ccccc1 Show InChI InChI=1S/C28H26N2O3/c1-31-25-10-9-20-14-24-22-16-27-26(32-18-33-27)15-21(22)11-13-30(24)17-23(20)28(25)29-12-5-8-19-6-3-2-4-7-19/h2-4,6-7,9-10,14-17H,5,8,11-13,18H2,1H3/p+1/b29-28-	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	785	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butylthiocholine chloride as substrate preincubated for 15 mins by Ellman's method				Eur J Med Chem 46: 5885-93 (2011) Article DOI: 10.1016/j.ejmech.2011.09.051 BindingDB Entry DOI: 10.7270/Q2Z60PGX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50358082 (CHEMBL1915196) Show SMILES COc1ccc2cc3-c4cc5OCOc5cc4CCn3cc2\c1=[NH+]\CCCc1ccccc1 Show InChI InChI=1S/C28H26N2O3/c1-31-25-10-9-20-14-24-22-16-27-26(32-18-33-27)15-21(22)11-13-30(24)17-23(20)28(25)29-12-5-8-19-6-3-2-4-7-19/h2-4,6-7,9-10,14-17H,5,8,11-13,18H2,1H3/p+1/b29-28-	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	680	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine chloride substrate as substrate preincubated for 15 mins by Ellman's method				Eur J Med Chem 46: 5885-93 (2011) Article DOI: 10.1016/j.ejmech.2011.09.051 BindingDB Entry DOI: 10.7270/Q2Z60PGX
					More data for this Ligand-Target Pair