null

SMILES: CN1CCC=C(C1)c1nsnc1OCCCCNCCCCCCCCNc1c2CCCCc2nc2ccccc12

InChI Key: InChIKey=FWWHROPNFJVMDD-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50415472   

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))	BDBM50415472 (CHEMBL589978) Show SMILES CN1CCC=C(C1)c1nsnc1OCCCCNCCCCCCCCNc1c2CCCCc2nc2ccccc12 |c:4| Show InChI InChI=1S/C33H48N6OS/c1-39-23-14-15-26(25-39)31-33(38-41-37-31)40-24-13-12-21-34-20-10-4-2-3-5-11-22-35-32-27-16-6-8-18-29(27)36-30-19-9-7-17-28(30)32/h6,8,15-16,18,34H,2-5,7,9-14,17,19-25H2,1H3,(H,35,36)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	26.3	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE by Ellman's method				J Med Chem 53: 2094-103 (2010) Article DOI: 10.1021/jm901616h BindingDB Entry DOI: 10.7270/Q2KW5H8J
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50415472 (CHEMBL589978) Show SMILES CN1CCC=C(C1)c1nsnc1OCCCCNCCCCCCCCNc1c2CCCCc2nc2ccccc12 |c:4| Show InChI InChI=1S/C33H48N6OS/c1-39-23-14-15-26(25-39)31-33(38-41-37-31)40-24-13-12-21-34-20-10-4-2-3-5-11-22-35-32-27-16-6-8-18-29(27)36-30-19-9-7-17-28(30)32/h6,8,15-16,18,34H,2-5,7,9-14,17,19-25H2,1H3,(H,35,36)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	13.5	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of BChE from equine serum by Ellman's method				J Med Chem 53: 2094-103 (2010) Article DOI: 10.1021/jm901616h BindingDB Entry DOI: 10.7270/Q2KW5H8J
					More data for this Ligand-Target Pair