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2000
Volume 4, Issue 2
  • ISSN: 1872-3128
  • E-ISSN: 1874-0758

Abstract

Imiloxan is an alpha2 adrenoceptor antagonist and was developed for depression in the 1980's. In Phase 1 clinical trials imiloxan dosing led to hypersensitivity reactions; the molecule's development was discontinued. The present study revisits the in vitro metabolism of imiloxan using modern analytical methods. Human and rat liver microsomes convert imiloxan into a variety of metabolites many of which are unstable and or reactive. Imiloxan also yields high protein covalent binding in microsomal assays. Imiloxan is a useful test molecule for defining the relationship between liver covalent binding and idiosyncratic toxicity.

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/content/journals/dml/10.2174/187231210791292753
2010-04-01
2025-09-04
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/content/journals/dml/10.2174/187231210791292753
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  • Article Type:
    Research Article
Keyword(s): Imiloxan; mass spectrometry; metabolism; reactive metabolite
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