Piperidine analogues of D-galactose as potent inhibitors of alpha-galactosidase: Synthesis by stannane-mediated hydroxymethylation of 5-azido-1,4-lactones. Structural relationships between D-galactosidase and L-rhamnosidase inhibitors

Παρόμοια τεκμήρια

• The synthesis of deoxygalactostatin and 2,6 imino-heptitol derivatives via stannane mediated hydroxymethylation of 5-azido-1,4-lactones
  ανά: Shilvock, J, κ.ά.
  Έκδοση: (1998)
• Looking glass inhibitors: both enantiomeric N-benzyl derivatives of 1,4-dideoxy-1,4-imino-D-lyxitol [a potent competitive inhibitor of alpha-D-galactosidase] and of 1,4-dideoxy-1,4-imino-L-lyxitol [a weak competitive inhibitor of alpha-D-galactosidase] inhibit naringinase, an alpha-L-rhamnosidase competitively
  ανά: Mercer, T, κ.ά.
  Έκδοση: (2009)
• Synthesis of lipophilic 1-deoxygalactonojirimycin derivatives as D-galactosidase inhibitors
  ανά: Georg Schitter, κ.ά.
  Έκδοση: (2010-03-01)
• Synthesis of homorhamnojirimycins and related trihydroxypipecolic acid derivatives via divergent bicyclic amino lactone intermediates: Inhibition of naringinase (L-rhamnosidase) and dTDP-rhamnose biosynthesis
  ανά: Shilvock, J, κ.ά.
  Έκδοση: (1999)
• Hydrolysis of lactose with -D-galactosidase
  ανά: Vesna Stehlik-Tomas, κ.ά.
  Έκδοση: (2001-06-01)