null

SMILES: O=C1c2ccccc2-c2nccc3c(OCCN4CCCCC4)ccc1c23

InChI Key: InChIKey=LZRZFBQWWOJNLQ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50342764   

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))	BDBM50342764 (4-(2-(Piperidin-1-yl)ethoxy)-7H-dibenzo[de,h]quino...) Show SMILES O=C1c2ccccc2-c2nccc3c(OCCN4CCCCC4)ccc1c23 Show InChI InChI=1S/C23H22N2O2/c26-23-17-7-3-2-6-16(17)22-21-18(10-11-24-22)20(9-8-19(21)23)27-15-14-25-12-4-1-5-13-25/h2-3,6-11H,1,4-5,12-15H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.21E+3	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 BChE by Ellman's method				Eur J Med Chem 46: 1572-81 (2011) Article DOI: 10.1016/j.ejmech.2011.02.005 BindingDB Entry DOI: 10.7270/Q2TM7BFW
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50342764 (4-(2-(Piperidin-1-yl)ethoxy)-7H-dibenzo[de,h]quino...) Show SMILES O=C1c2ccccc2-c2nccc3c(OCCN4CCCCC4)ccc1c23 Show InChI InChI=1S/C23H22N2O2/c26-23-17-7-3-2-6-16(17)22-21-18(10-11-24-22)20(9-8-19(21)23)27-15-14-25-12-4-1-5-13-25/h2-3,6-11H,1,4-5,12-15H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	88	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 by Ellman's method				Eur J Med Chem 46: 1572-81 (2011) Article DOI: 10.1016/j.ejmech.2011.02.005 BindingDB Entry DOI: 10.7270/Q2TM7BFW
					More data for this Ligand-Target Pair