Glutathione conjugates of misonidazole

Biochem Biophys Res Commun. 1983 May 16;112(3):1013-20. doi: 10.1016/0006-291x(83)91719-9.

Abstract

The hydroxylamine derivative of misonidazole reacts with glutathione under physiological conditions to form two isomeric conjugates. Based on physical and chemical properties, the two conjugates have been identified as 1-[2-amino-(4-glutathion-S-yl)-1-imidazolyl]-3-methoxypropanol and 1-[2-amino-(5-glutathion-S-yl)-1-imidazolyl]-3-methoxypropanol. The formation of the glutathione conjugates of reduced misonidazole offers a molecular mechanism for the depletion of GSH in mammalian cells after exposure to misonidazole under hypoxic conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Gas Chromatography-Mass Spectrometry
  • Glutathione / metabolism*
  • Magnetic Resonance Spectroscopy
  • Misonidazole / metabolism*
  • Nitroimidazoles / metabolism*
  • Oxidation-Reduction

Substances

  • Nitroimidazoles
  • Misonidazole
  • Glutathione