1. Academic Validation
  2. Testosterone 1 beta-hydroxylation by human cytochrome P450 3A4

Testosterone 1 beta-hydroxylation by human cytochrome P450 3A4

  • Eur J Biochem. 2004 Oct;271(19):3962-9. doi: 10.1111/j.1432-1033.2004.04339.x.
Joel A Krauser 1 Markus Voehler Li-Hong Tseng Alexandre B Schefer Markus Godejohann F Peter Guengerich
Affiliations

Affiliation

  • 1 Department of Biochemistry and Center in Molecular Toxicology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146, USA.
Abstract

Human Cytochrome P450 3A4 forms a series of minor testosterone hydroxylation products in addition to 6 beta-hydroxytestosterone, the major product. One of these, formed at the next highest rate after the 6 beta- and 2 beta-hydroxy products, was identified as 1 beta-hydroxytestosterone. This product was characterized from a mixture of testosterone oxidation products using an HPLC-solid phase extraction-cryoprobe NMR/time-of-flight mass spectrometry system, with an estimated total of approximately 6 microg of this product. Mass spectrometry established the formula as C(19)H(29)O(3) (MH(+) 305.2080). The 1-position of the added hydroxyl group was established by correlated spectroscopy and heteronuclear spin quantum correlation experiments, and the beta-stereochemistry of the added hydroxyl group was assigned with a nuclear Overhauser correlated spectroscopy experiment (1 alpha-H). Of several human P450s examined, only P450 3A4 formed this product. The product was also formed in human liver microsomes.

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