PubMed · 4689016
Pyrethroid insecticides: esterase cleavage in relation to selective toxicity.
Abstract
The ester group of primary alcohol chrysanthemates is cleaved by mouse hepatic microsomal esterases, more rapidly for the (+)-trans than for the (+)-cis isomers. Substrate-specificity and inhibition studies in vivo establish that these pyrethroid-hydrolyzing esterases probably contribute to the low mammalian toxicity of bioresmethrin and other (+)-trans chrysanthemate insecticide chemicals derived from primary alcohols.
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C O Abernathy, J E Casida. 1973-03-23. Pyrethroid insecticides: esterase cleavage in relation to selective toxicity.. https://doi.org/10.1126/science.179.4079.1235
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