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Inhibitor Report for: Dialifor-oxon

General
Type Organophosphate, Insecticide, Isoindole, Indole, Sulfur Compound
Chemical_Nomenclature 2-(2-chloro-1-diethoxyphosphorylsulfanyl-ethyl)isoindole-1,3-dione
Canonical SMILES CCOP(=O)(OCC)SC(CCl)N1C(=O)C2=CC=CC=C2C1=O
InChI InChI=1S/C14H17ClNO5PS/c1-3-20-22(19,21-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3
InChIKey DGFSZLIRMFVRBS-UHFFFAOYSA-N
Other name(s) 18776-60-8 ; Phosphorothioic acid, S-(2-chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl) O,O-diethyl ester
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MW|377.781
Formula|C14H17ClNO5PS
CAS_number|
PubChem|167745
UniChem|DGFSZLIRMFVRBS-UHFFFAOYSA-N
IUPHAR|
Wikipedia|

Target
Families | Dialifor-oxon ligand of proteins in family: ACHE

References:
Search PubMed for references concerning: Dialifor-oxon
    Title: Environmental fate of dialifor and formation of its oxygen analogue following application on grape vines in the San Joaquin Valley, California
    Winterlin W, Walker G, Hall G, McFarland J, Mourer C
    Ref: Journal of Agricultural and Food Chemistry, 28:1078, 1980 : PubMed

            

    Title: Dislodgable residues of dialifor and phosalone and their oxygen analogs following a reported worker-injury incident in the San Joaquin Valley, California
    Winterlin W, Kilgore W, Mourer C, Mull R, Walker G, Knaak J, Maddy K
    Ref: Bulletin of Environmental Contamination & Toxicology, 20:255, 1978 : PubMed