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 language | English (US) |
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Pages (from-to) | 289-294 |
Number of pages | 6 |
Journal | Drug Metabolism and Disposition |
Volume | 8 |
Issue number | 5 |
State | Published - 1980 |
Externally published | Yes |
ASJC Scopus subject areas
- Pharmacology
- Pharmaceutical Science