Synthesis and evaluation of glucocerebrosidase inhibitory activity of anhydro deoxyinositols from (+)-epi- and (-)-vibo-quercitols

Bioorg Med Chem Lett. 1999 Jun 7;9(11):1493-8. doi: 10.1016/s0960-894x(99)00223-1.

Abstract

Twelve 1,2- and 2,3-anhydro-1,2,3,4,5-cyclohexanepentols were synthesized from (+)-epi- and (-)-vibo-quercitols, readily available by bioconversion of myo-inositol, and assayed for inhibitory activity against glucocerebrosidase (mouse liver). Among them 1L-1,2-anhydro-1,2,4/3,5-cyclohexanepentol, the 3-deoxy derivative of the irreversible inhibitor conduritol B epoxide (CBE), has been demonstrated to be a highly potent and specific inhibitor, almost comparable to the parent compound.

MeSH terms

  • Animals
  • Glucosylceramidase / antagonists & inhibitors*
  • Inositol / analogs & derivatives*
  • Inositol / chemical synthesis*
  • Liver / enzymology
  • Magnetic Resonance Spectroscopy
  • Mice
  • Models, Chemical

Substances

  • Inositol
  • Glucosylceramidase