1980
DOI: 10.1021/jf60232a007
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Metabolism of carbamate insecticide thiofanox in rats

Abstract: N-dealkylated metabolites, deethylatrazine and deisopropylatrazine, are further hydrolyzed to the corresponding hydroxy analogues. ACKNOWLEDGMENTThe skilled technical assistance of N.

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Cited by 2 publications
(2 citation statements)
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“…Although carbamate insecticides are relatively less pharmacologically toxic as anticholinesterase agents in contrast to organophosphorus compounds, The chemical structure, metabolism and distribution on of carbamates as well as its insecticidal activity were extensively studied (Chin et al, 1980 andOsman et al, 1983).…”
Section: Introductionmentioning
confidence: 99%
“…Although carbamate insecticides are relatively less pharmacologically toxic as anticholinesterase agents in contrast to organophosphorus compounds, The chemical structure, metabolism and distribution on of carbamates as well as its insecticidal activity were extensively studied (Chin et al, 1980 andOsman et al, 1983).…”
Section: Introductionmentioning
confidence: 99%
“…carbonyl]oxime (P2). Metabolic study of P in rats (Chin et al, 1980) showed that P2 was hydroxylated further to form 3,3-dimethyl-l-(methylsulfonyl)-2-butanone 0-[(hydroxymethylamino)carbonyl]oxime (P2OH).…”
mentioning
confidence: 99%