Stereoisomers of Ketoconazole: Preparation and Biological Activity

J Med Chem. 1992 Jul 24;35(15):2818-25. doi: 10.1021/jm00093a015.

Abstract

The four stereoisomers of the antifungal agent ketoconazole (1) were prepared and evaluated for their selectivity in inhibiting a number of cytochrome P-450 enzymes. Large differences in selectivity among the isomers were observed for inhibition of the cytochromes P-450 involved in steroid biosynthesis, whereas little differences was observed for inhibition of those associated with hepatic drug metabolism. The cis-(2S,4R) isomer 2 was the most effective against rat lanosterol 14 alpha-demethylase, (2S,4R)-2 greater than (2R,4S)-4 much greater than (2R,4R)-3 = (2S,4S)-5, and progesterone 17 alpha,20-lyase, (2S,4R)-2 much greater than (2S,4S)-5 greater than (2R,4R)-3 = (2R,4S)-4, whereas the cis-(2R,4S) isomer 4 was more effective against cholesterol 7 alpha-hydroxylase, (2R,4S)-4 greater than (2S,4S)-5 greater than (2R,4R)-3, greater than (2S,4R)-2, and the trans-(2S,4S) isomer 5 was the most effective against aromatase, (2S,4R)-5 much greater than (2R,4R)-3 = (2R,4S)-4 greater than (2S,4R)-2. The cis-(2S,4R) and trans-(2R,4R) isomers 2 and 3 are equipotent in inhibiting corticoid 11 beta-hydroxylase and much more effective than their antipodes. Little selectivity was observed for inhibition of cholesterol side chain cleavage or xenobiotic hydroxylase. These data indicate that the affinity of azoles for cytochrome P-450 enzymes involved in steroid synthesis is highly dependent on the stereochemistry of the entire molecule, whereas binding to drug metabolizing enzymes is a less selective process.

MeSH terms

  • Adrenal Glands / drug effects
  • Adrenal Glands / enzymology
  • Animals
  • Cytochrome P-450 Enzyme Inhibitors
  • Female
  • Humans
  • Ketoconazole / chemical synthesis*
  • Ketoconazole / pharmacology
  • Male
  • Microsomes / drug effects
  • Microsomes / enzymology
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology
  • Placenta / drug effects
  • Placenta / enzymology
  • Pregnancy
  • Rats
  • Stereoisomerism
  • Swine
  • Testis / drug effects
  • Testis / enzymology

Substances

  • Cytochrome P-450 Enzyme Inhibitors
  • Ketoconazole