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- W2037697996 abstract "[14C]Flamprop-methyl administered orally to rats (3-4 mg kg−1 body weight) was excreted mostly via the faeces (78.7 and 61.6% in males and females, respectively). Elimination was rapid and 90% of the dose of 14C was excreted in faeces and urine 0-48 h after dosing. The distribution of 14C between faeces and urine was different in males and females. No expired [14C]carbon dioxide was detected and less than 2% of the dose remained in the animals 4 days after dosing. The predominant metabolic pathway was hydrolysis of the ester bond to afford the carboxylic acid which was excreted unchanged and as its glucuronide conjugate. Aromatic hydroxylation occurred at the para- and meta-positions of the N-benzoyl ring. N-(3)-Chloro- 4-fluorophenyl-N-(3,4-dihydroxybenzoyl)-DL-alaninate was also formed. This hydroxylated form of flamprop-methyl was partially O-methylated at the 3-hydroxy group. Flamprop-methyl was also metabolised and eliminated rapidly by dogs, mice and rabbits. The last of these three species afforded very little aromatic hydroxylation and also differed from the others in that the metabolites were eliminated mostly in the urine. Aromatic hydroxylation lay in the order: male rat = female rat > dog= mouse>rabbit (female)." @default.
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- W2037697996 date "1980-12-01" @default.
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- W2037697996 title "The metabolism of the herbicide flamprop-methyl in rats and some comparative data for dogs, mice and rabbits" @default.
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- W2037697996 doi "https://doi.org/10.1002/ps.2780110605" @default.
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