Formation of pentachlorothioanisole from N-acetyl-S-(pentachlorophenyl) cysteine in blood and liver of rats "in vivo"

Life Sci. 1983 Oct 3;33(14):1427-31. doi: 10.1016/0024-3205(83)90826-3.

Abstract

Studies on the biotransformation of N-acetyl-S-(pentachlorophenyl) cysteine, a mutual polar metabolite of the lipophilic fungicides pentachloronitrobenzene and hexachlorobenzene, showed metabolic conversions in rats. The rate of its metabolism, leading in return to more lipophilic and toxic products (1) was investigated by determination of pentachlorothioanisole, its major metabolite in blood and liver of rats. The metabolic rate was found to be very small.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine / analogs & derivatives*
  • Acetylcysteine / metabolism
  • Animals
  • Biotransformation
  • Chlorobenzenes / biosynthesis*
  • Female
  • Liver / metabolism*
  • Male
  • Rats
  • Rats, Inbred Strains
  • Sex Characteristics
  • Time Factors

Substances

  • Chlorobenzenes
  • pentachlorophenylmercapturic acid
  • pentachloromethylthiobenzene
  • Acetylcysteine