Monooxygenation of N-acetylhistamine mediated by L-ascorbate

Biochim Biophys Acta. 1989 May 31;991(2):377-9. doi: 10.1016/0304-4165(89)90131-1.

Abstract

In the presence of molecular oxygen and a catalytic amount of copper(II) ion, ascorbate almost completely degraded histamine (approx. 72%). The reaction was shown to occur at the imidazole group but not at the primary amino group in histamine. 4-[2-(Acetylamino)ethyl]-2,3-dihydroimidazol-2-one, a monooxygenated form of N-acetylhistamine, was first isolated as the primary product.

MeSH terms

  • Ascorbic Acid*
  • Chromatography, High Pressure Liquid
  • Histamine / analogs & derivatives*
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Oxidation-Reduction

Substances

  • N-acetylhistamine
  • Histamine
  • Ascorbic Acid