Stereodependent bioactivation of R(+)-ethyl S-propyl methylphosphonothioate: Is the S-oxide the active metabolite?-Reference-Cited by-同舟云学术

Stereodependent bioactivation of R(+)-ethyl S-propyl methylphosphonothioate: Is the S-oxide the active metabolite?

Published:1985-08 Issue:1 Volume:24 Page:53-60
ISSN:0048-3575
Container-title:Pesticide Biochemistry and Physiology
language:en
Short-container-title:Pesticide Biochemistry and Physiology

Author:

French M.C.,Hall C.R.,Harrison J.M.,Inch T.D.,Sellers D.J.,Smith A.P.,Upshall D.G.,Watts P.

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Agronomy and Crop Science,General Medicine

Reference14 articles.

1. Differences between some biological properties of enantiomers of alkyl S-alkyl methylphosphonothioates;Hall;J. Pharm. Pharmacol,1977

2. Resolution and biological activity of the chiral isomers of O-(4-bromo-2-chlorophenyl) O-ethyl-S-propyl phosphonothioate (Profenofos Insecticide);Leader;J. Agric. Food Chem,1982

3. Oxidative bioactivation of S-alkyl phosphonothioate pesticides: Stereospecificity of profenofos insecticide activation;Wing;Science,1983

4. K. D. Wing, A. H. Glickman, and J. E. Casida, Structural requirements for oxidative bioactivation and ageing of the inhibited acetylcholinesterase, in press.

5. Oxidative conversion of phosphonothioalates to phosphenyloxysulphonates probably via phosphonothioalate S-oxides;Segall;Tetrahedron Lett,1982

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