A Complete Study of Farrerol Metabolites Produced in Vivo and in Vitro

Molecules. 2019 Sep 24;24(19):3470. doi: 10.3390/molecules24193470.

Abstract

Although farrerol, a characteristically bioactive constituent of Rhododendron dauricum L., exhibits extensive biological and pharmacological activities (e.g., anti-oxidant, anti-immunogenic, and anti-angiogenic) as well as a high drug development potential, its metabolism remains underexplored. Herein, we employed ultra-high performance liquid chromatography/quadrupole time-of-flight mass spectrometry coupled with multiple data post-processing techniques to rapidly identify farrerol metabolites produced in vivo (in rat blood, bile, urine and feces) and in vitro (in rat liver microsomes). As a result, 42 in vivo metabolites and 15 in vitro metabolites were detected, and farrerol shown to mainly undergo oxidation, reduction, (de)methylation, glucose conjugation, glucuronide conjugation, sulfate conjugation, N-acetylation and N-acetylcysteine conjugation. Thus, this work elaborates the metabolic pathways of farrerol and reveals the potential pharmacodynamics forms of farrerol.

Keywords: UHPLC-Q-TOF-MS/MS; farrerol; in vitro; in vivo; metabolism; multiple data post-processing techniques.

MeSH terms

  • Chromatography, High Pressure Liquid*
  • Chromones / chemistry*
  • Chromones / metabolism*
  • Metabolic Detoxication, Phase I
  • Metabolic Detoxication, Phase II
  • Molecular Structure
  • Oxidation-Reduction
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization*
  • Tandem Mass Spectrometry*

Substances

  • Chromones
  • farrerol