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SMILES: COc1cccc2cc(oc12)C(=O)NCCCCCCNc1c2CCCc2nc2ccccc12

InChI Key: InChIKey=HDTGPJNBSTWCLU-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50138325   

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
Acetylcholinesterase (Homo sapiens (Human))	BDBM50138325 (CHEMBL3753508) Show SMILES COc1cccc2cc(oc12)C(=O)NCCCCCCNc1c2CCCc2nc2ccccc12 Show InChI InChI=1S/C28H31N3O3/c1-33-24-15-8-10-19-18-25(34-27(19)24)28(32)30-17-7-3-2-6-16-29-26-20-11-4-5-13-22(20)31-23-14-9-12-21(23)26/h4-5,8,10-11,13,15,18H,2-3,6-7,9,12,14,16-17H2,1H3,(H,29,31)(H,30,32)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.69E+3	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of recombinant human AChE using acetylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition by Ellman's ...				J Med Chem 59: 114-31 (2016) Article DOI: 10.1021/acs.jmedchem.5b01119 BindingDB Entry DOI: 10.7270/Q2S75J5X
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50138325 (CHEMBL3753508) Show SMILES COc1cccc2cc(oc12)C(=O)NCCCCCCNc1c2CCCc2nc2ccccc12 Show InChI InChI=1S/C28H31N3O3/c1-33-24-15-8-10-19-18-25(34-27(19)24)28(32)30-17-7-3-2-6-16-29-26-20-11-4-5-13-22(20)31-23-14-9-12-21(23)26/h4-5,8,10-11,13,15,18H,2-3,6-7,9,12,14,16-17H2,1H3,(H,29,31)(H,30,32)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	81	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of human serum BChE using butyrylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition by Ellman's metho...				J Med Chem 59: 114-31 (2016) Article DOI: 10.1021/acs.jmedchem.5b01119 BindingDB Entry DOI: 10.7270/Q2S75J5X
					More data for this Ligand-Target Pair