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SMILES: Cl.CN(C)c1ccc(cc1)C(=O)NCCCCNc1c2CCCCc2nc2ccccc12

InChI Key: InChIKey=SAXGCXXSOSTHKB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50114363   

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 (Electrophorus electricus (Electric eel))	BDBM50114363 (CHEMBL3604194) Show SMILES Cl.CN(C)c1ccc(cc1)C(=O)NCCCCNc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C26H32N4O.ClH/c1-30(2)20-15-13-19(14-16-20)26(31)28-18-8-7-17-27-25-21-9-3-5-11-23(21)29-24-12-6-4-10-22(24)25;/h3,5,9,11,13-16H,4,6-8,10,12,17-18H2,1-2H3,(H,27,29)(H,28,31);1H	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using ATC iodide substrate by Ellman's assay				Bioorg Med Chem 23: 5610-8 (2015) BindingDB Entry DOI: 10.7270/Q25T3N9G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50114363 (CHEMBL3604194) Show SMILES Cl.CN(C)c1ccc(cc1)C(=O)NCCCCNc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C26H32N4O.ClH/c1-30(2)20-15-13-19(14-16-20)26(31)28-18-8-7-17-27-25-21-9-3-5-11-23(21)29-24-12-6-4-10-22(24)25;/h3,5,9,11,13-16H,4,6-8,10,12,17-18H2,1-2H3,(H,27,29)(H,28,31);1H	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	295	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of acetylcholinesterase in human erythrocytes using acetylthiocholine iodide substrate by spectrophotometric Ellman's method				Bioorg Med Chem 23: 5610-8 (2015) BindingDB Entry DOI: 10.7270/Q25T3N9G
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50114363 (CHEMBL3604194) Show SMILES Cl.CN(C)c1ccc(cc1)C(=O)NCCCCNc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C26H32N4O.ClH/c1-30(2)20-15-13-19(14-16-20)26(31)28-18-8-7-17-27-25-21-9-3-5-11-23(21)29-24-12-6-4-10-22(24)25;/h3,5,9,11,13-16H,4,6-8,10,12,17-18H2,1-2H3,(H,27,29)(H,28,31);1H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Medical College Curated by ChEMBL					Assay Description Inhibition of equine serum BChE using ATC iodide substrate by Ellman's assay				Bioorg Med Chem 23: 5610-8 (2015) BindingDB Entry DOI: 10.7270/Q25T3N9G
					More data for this Ligand-Target Pair