null

SMILES: CCN(CC)CCSC(N=O)c1nc(Cc2ccccc2)no1

InChI Key: InChIKey=OHCDZUAEPDMQDQ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50025239   

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))	BDBM50025239 (3-Benzyl-N-hydroxy-[1,2,4]oxadiazole-5-carboximido...) Show SMILES CCN(CC)CCSC(N=O)c1nc(Cc2ccccc2)no1 Show InChI InChI=1S/C16H22N4O2S/c1-3-20(4-2)10-11-23-16(18-21)15-17-14(19-22-15)12-13-8-6-5-7-9-13/h5-9,16H,3-4,10-12H2,1-2H3	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	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro reversible inhibition of eel acetylcholinesterase.				J Med Chem 29: 2174-83 (1986) BindingDB Entry DOI: 10.7270/Q2VQ31QK
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50025239 (3-Benzyl-N-hydroxy-[1,2,4]oxadiazole-5-carboximido...) Show SMILES CCN(CC)CCSC(N=O)c1nc(Cc2ccccc2)no1 Show InChI InChI=1S/C16H22N4O2S/c1-3-20(4-2)10-11-23-16(18-21)15-17-14(19-22-15)12-13-8-6-5-7-9-13/h5-9,16H,3-4,10-12H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro reversible inhibition of eel acetylcholinesterase.				J Med Chem 29: 2174-83 (1986) BindingDB Entry DOI: 10.7270/Q2VQ31QK
					More data for this Ligand-Target Pair