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- W2026396988 abstract "Organophosphorus insecticides with substituted or unsubstituted 4-nitrophenyl ester structure were examined for their metabolism in vitro by microsomes of rat and rabbit livers and of housefly abdomens. Compounds studied included methyl parathion, parathion, n -propyl parathion, iso -propyl parathion, dicapthon, Sumithion, Chlorthion and O -ethyl O -4-nitrophenyl phenylphosphonothioate and their P O analogs. All P S compounds were metabolized via two oxidative pathways, activation to P O analogs and cleavage at the aryl phosphate bond. These reactions occurred only in the presence of NADPH 2 and O 2 . The oxidative cleavage also occurred with one P O compound, n -propyl paraoxon." @default.
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- W2026396988 date "1968-08-01" @default.
- W2026396988 modified "2023-09-25" @default.
- W2026396988 title "Degradation and activation of parathion analogs by microsomal enzymes" @default.
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- W2026396988 doi "https://doi.org/10.1016/0006-2952(68)90211-6" @default.
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