null

SMILES: CN1CCN(CCCOc2ccc3C(=O)c4ccccc4-c4nccc2c34)CC1

InChI Key: InChIKey=LOIVFJYITDDQIW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50342767   

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))	BDBM50342767 (4-(3-(4-Methylpiperazin-1-yl)propoxy)-7H-dibenzo[d...) Show SMILES CN1CCN(CCCOc2ccc3C(=O)c4ccccc4-c4nccc2c34)CC1 Show InChI InChI=1S/C24H25N3O2/c1-26-12-14-27(15-13-26)11-4-16-29-21-8-7-20-22-19(21)9-10-25-23(22)17-5-2-3-6-18(17)24(20)28/h2-3,5-10H,4,11-16H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.50E+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))	BDBM50342767 (4-(3-(4-Methylpiperazin-1-yl)propoxy)-7H-dibenzo[d...) Show SMILES CN1CCN(CCCOc2ccc3C(=O)c4ccccc4-c4nccc2c34)CC1 Show InChI InChI=1S/C24H25N3O2/c1-26-12-14-27(15-13-26)11-4-16-29-21-8-7-20-22-19(21)9-10-25-23(22)17-5-2-3-6-18(17)24(20)28/h2-3,5-10H,4,11-16H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	405	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