Studies on the chiral isomers of fonofos and fonofos oxon: I. Toxicity and antiesterase activities

Abstract

The toxicity of the ( R) P and ( S) P chiral isomers and racemates of fonofos and fonofos oxon to insects and white mice were determined. ( R) P-Fonofos and ( S) P-fonofos oxon were 2- to 12-fold more toxic to house flies, mosquito larvae, and mice than were the corresponding enantiomers. The racemates were intermediate in toxicity. Stereoselectivity also was observed in the in vitro inhibition of house fly-head and bovine erythrocyte acetylcholinesterase, horse serum cholinesterase, chymotrypsin, trypsin, and a variety of esterases. In all cases the ( S) P-oxon was a more potent inhibitor than the ( R) P-oxon with k 1 ratios of (S) P (R) P ranging from 4- to 60-fold. Further, differences in levels of house fly-head, mouse brain, and blood cholinesterase obtained from house flies and mice treated with the enantiomers and racemates of fonofos and fonofos oxon were observed. Differences in toxicity of the enantiomers and racemates to house flies and mice were more closely related to in vivo than to in vitro cholinesterase inhibition.