Inhibition of naringinase (L-rhamnosidase) by piperidine analogues of L-rhamnose: Scaffolds for libraries incorporating trihydroxypipecolic acids

Samankaltaisia teoksia

• Synthesis of homorhamnojirimycins and related trihydroxypipecolic acid derivatives via divergent bicyclic amino lactone intermediates: Inhibition of naringinase (L-rhamnosidase) and dTDP-rhamnose biosynthesis
  Tekijä: Shilvock, J, et al.
  Julkaistu: (1999)
• 2-hydroxycastanospermines (dihydroxy-L-swainsonines) from octonolactones: Inhibition of naringinase (L-rhamnosidase)
  Tekijä: Bell, A, et al.
  Julkaistu: (1996)
• L-(+)-swainsonine and other pyrrolidine inhibitors of naringinase: Through an enzymic looking glass from D-mannosidase to L-rhamnosidase?
  Tekijä: Davis, B, et al.
  Julkaistu: (1996)
• Divergent intermediates for the generation of libraries of L-rhamnose mimics
  Tekijä: Smith, M, et al.
  Julkaistu: (1996)
• Synthesis of the naringinase inhibitors L-swainsonine and related 6-C-methyl-L-swainsonine analogues: (6R)-C-methyl-L-swainsonine is a more potent inhibitor of L-rhamnosidase by an order of magnitude than L-swainsonine
  Tekijä: Hakansson, A, et al.
  Julkaistu: (2008)