3-Hydroxyacetaminophen: A microsomal metabolite of acetaminophen. Evidence against an epoxide as the reactive metabolite of acetaminophen

  • J. A. Hinson
  • , L. R. Pohl
  • , T. J. Monks
  • , J. R. Gillette
  • , F. P. Guengerich

Research output: Contribution to journalArticlepeer-review

77 Scopus citations

Abstract

3-Hydroxyacetaminophen has been isolated and identified as a microsomal metabolite of acetaminophen. Analysis of the metabolite by gas chromatography-mass spectrometry revealed that the metabolite had a molecular ion and fragmentation pattern identical to that of authentic 3-hydroxyacetaminophen. Glutathione and ascorbic acid blocked covalent binding of reactive metabolite(s) to protein but did not block the formation of 3-hydroxyacetaminophen. Moreover, epoxide hydrolase did not block covalent binding of the reactive metabolite(s) to protein. Thus, the reactive metabolite apparently is not an epoxide substrate of the hydrolase, nor are 3-hydroxyacetaminophen and the reactive metabolites(s) formed from a common intermediate.

Original languageEnglish (US)
Pages (from-to)289-294
Number of pages6
JournalDrug Metabolism and Disposition
Volume8
Issue number5
StatePublished - 1980
Externally publishedYes

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

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