null

SMILES: CCOC(=O)\C=C\c1ccc(OCCCCCCN(CC)CC)c(OC)c1

InChI Key: InChIKey=PQAFELCHIANEDB-FYWRMAATSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50232229   

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 (Homo sapiens (Human))	BDBM50232229 (CHEMBL4072405) Show SMILES CCOC(=O)\C=C\c1ccc(OCCCCCCN(CC)CC)c(OC)c1 Show InChI InChI=1S/C22H35NO4/c1-5-23(6-2)16-10-8-9-11-17-27-20-14-12-19(18-21(20)25-4)13-15-22(24)26-7-3/h12-15,18H,5-11,16-17H2,1-4H3/b15-13+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Hu'nan University Curated by ChEMBL					Assay Description Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann method				Eur J Med Chem 126: 810-822 (2017) BindingDB Entry DOI: 10.7270/Q2HH6N9M
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50232229 (CHEMBL4072405) Show SMILES CCOC(=O)\C=C\c1ccc(OCCCCCCN(CC)CC)c(OC)c1 Show InChI InChI=1S/C22H35NO4/c1-5-23(6-2)16-10-8-9-11-17-27-20-14-12-19(18-21(20)25-4)13-15-22(24)26-7-3/h12-15,18H,5-11,16-17H2,1-4H3/b15-13+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.90	n/a	n/a	n/a	n/a	n/a	n/a
Hu'nan University Curated by ChEMBL					Assay Description Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann method				Eur J Med Chem 126: 810-822 (2017) BindingDB Entry DOI: 10.7270/Q2HH6N9M
					More data for this Ligand-Target Pair