Hydroxylation of progesterone by Cephalosporium aphidicola

Phytochemistry. 1994 Oct;37(3):723-6. doi: 10.1016/s0031-9422(00)90346-7.

Abstract

The fungus, Cephalosporium aphidicola, has been shown to hydroxylate progesterone predominantly at the 6 beta- and 11 alpha-positions. Minor metabolites include testosterone acetate, the 20(R)-alcohol and 12 beta, 17 alpha-dihydroxy-progesterone. The sequence involves hydroxylation at 11 alpha and then 6 beta. The hydroxylations of 11 alpha- and 17 alpha-hydroxyprogesterone and of 9 beta, 10 alpha-retroprogesterone have also been examined in the light of these results.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acremonium / metabolism*
  • Chromatography, Thin Layer
  • Hydroxylation
  • Magnetic Resonance Spectroscopy
  • Progesterone / metabolism*
  • Spectrophotometry, Infrared

Substances

  • Progesterone