Literature DB >> 27918992

Investigation of the metabolites of the HIF stabilizer FG-4592 (roxadustat) in five different in vitro models and in a human doping control sample using high resolution mass spectrometry.

Annelie Hansson1, Mario Thevis2, Holly Cox3, Geoff Miller4, Daniel Eichner5, Ulf Bondesson6, Mikael Hedeland7.   

Abstract

FG-4592 is a hypoxia-inducible factor (HIF) stabilizer, which can increase the number of red blood cells in the body. It has not been approved by regulatory authorities, but is available for purchase on the Internet. Due to its ability to improve the oxygen transportation mechanism in the body, FG-4592 is of interest for doping control laboratories, but prior to this study, little information about its metabolism was available. In this study, the metabolism of FG-4592 was investigated in a human doping control sample and in five in vitro models: human hepatocytes and liver microsomes, equine liver microsomes and S9 fraction and the fungus Cunninghamella elegans. By using liquid chromatography coupled to a Q-TOF mass spectrometer operated in MSE and MSMS modes, twelve different metabolites were observed for FG-4592. One monohydroxylated metabolite was detected in both the human and equine liver microsome incubations. For the fungus Cunninghamella elegans eleven different metabolites were observed of which the identical monohydroxylated metabolite had the highest response. This rich metabolic profile and the higher levels of metabolites produced by Cunninghamella elegans demonstrates its usefulness as a metabolite producing medium. In the doping control urine sample, one metabolite, which was the result of a direct glucuronidation, was observed. No metabolites were detected in neither the human hepatocyte nor in the equine liver S9 fraction incubates.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Drug metabolism; FG-4592; High resolution mass spectrometry

Mesh:

Substances:

Year:  2016        PMID: 27918992     DOI: 10.1016/j.jpba.2016.11.041

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  2 in total

1.  Metabolic Profile of Synthetic Cannabinoids 5F-PB-22, PB-22, XLR-11 and UR-144 by Cunninghamella elegans.

Authors:  Shimpei Watanabe; Unnikrishnan Kuzhiumparambil; My Ann Nguyen; Jane Cameron; Shanlin Fu
Journal:  AAPS J       Date:  2017-04-28       Impact factor: 4.009

2.  Structural Basis of Prolyl Hydroxylase Domain Inhibition by Molidustat.

Authors:  William D Figg; Michael A McDonough; Rasheduzzaman Chowdhury; Yu Nakashima; Zhihong Zhang; James P Holt-Martyn; Alen Krajnc; Christopher J Schofield
Journal:  ChemMedChem       Date:  2021-04-09       Impact factor: 3.540

  2 in total

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