1984
DOI: 10.1016/0048-3575(84)90103-2
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The effect of isomalathion and O,S,S-trimethyl phosphorodithioate on the in vivo metabolism of malathion in rats

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Cited by 10 publications
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“…Isomalathion and OSS are potent inhibitors of rat plasma, liver and kidney malathion carboxylesterases. In consequence less malathion diacid, but more amonoacid and malaoxon metabolites are excreted compared with control animals, suggesting an increased production of malaoxon in the presence of these impurities (Ryan and Fukuto 1984 Although they are poor AChE inhibitors and poor alkylating agents per se, trimethyl phosphorothioates have interesting toxicological properties of their own, producing delayed deaths in rats, associated with lung damage (Aldridge et al 1984).…”
mentioning
confidence: 96%
“…Isomalathion and OSS are potent inhibitors of rat plasma, liver and kidney malathion carboxylesterases. In consequence less malathion diacid, but more amonoacid and malaoxon metabolites are excreted compared with control animals, suggesting an increased production of malaoxon in the presence of these impurities (Ryan and Fukuto 1984 Although they are poor AChE inhibitors and poor alkylating agents per se, trimethyl phosphorothioates have interesting toxicological properties of their own, producing delayed deaths in rats, associated with lung damage (Aldridge et al 1984).…”
mentioning
confidence: 96%