Synthesis and glycosidase inhibition of N-substituted derivatives of 1,4-dideoxy-1,4-imino-d-mannitol (DIM)

Org Biomol Chem. 2020 Feb 7;18(5):999-1011. doi: 10.1039/c9ob02029b. Epub 2020 Jan 16.

Abstract

N-Substituted derivatives of 1,4-dideoxy-1,4-imino-d-mannitol (DIM), the pyrrolidine core of swainsonine, have been synthesized efficiently and stereoselectively from d-mannose with 2,3:5,6-di-O-isopropylidene DIM (10) as a key intermediate. These N-substituted derivatives include N-alkylated, N-alkenylated, N-hydroxyalkylated and N-aralkylated DIMs with the carbon number of the alkyl chain ranging from one to nine. The obtained 33 N-substituted DIM derivatives were assayed against various glycosidases, which allowed a systematic evaluation of their glycosidase inhibition profiles. Though N-substitution of DIM decreased their α-mannosidase inhibitory activities, some of the derivatives showed significant inhibition of other glycosidases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enzyme Inhibitors / chemical synthesis*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Glycoside Hydrolases / antagonists & inhibitors*
  • Glycoside Hydrolases / metabolism
  • Humans
  • Imino Furanoses / chemical synthesis
  • Imino Furanoses / chemistry
  • Imino Furanoses / pharmacology
  • Inhibitory Concentration 50
  • Mannitol / analogs & derivatives*
  • Mannitol / chemical synthesis
  • Mannitol / chemistry
  • Mannitol / pharmacology
  • Rats
  • Swainsonine / chemistry

Substances

  • Enzyme Inhibitors
  • Imino Furanoses
  • Mannitol
  • 1,4-dideoxy-1,4-iminomannitol
  • Glycoside Hydrolases
  • Swainsonine