59997-96-5

Upstream product

• 22796-65-2 p-nitrophenyl α-L-arabinofuranoside 
• 1357007-67-0 benzyl 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->5)-α-L-arabinofuranoside 
• 2001-96-9 p-nitrophenyl β-D-xylopyranoside 

Relevant academic research and scientific papers

Exploiting sp2-Hybridisation in the Development of Potent 1,5-α-l-Arabinanase Inhibitors

The synthesis of potent inhibitors of GH93 arabinanases as well as a synthesis of a chromogenic substrate to measure GH93 arabinanase activity are described. An insight into the reasons behind the potency of the inhibitors was gained through X-ray crystallographic analysis of the arabinanase Arb93A from Fusarium graminearum. These compounds lay a foundation for future inhibitor development as well as for the use of the chromogenic substrate in biochemical studies of GH93 arabinanases.

Synthesis of α-L-Araf and β-D-Galf series furanobiosides using mutants of a GH51 α-L-arabinofuranosidase

The GH-51 α-L-arabinofuranosidase from Thermobacillus xylanilyticus (TxAbf) possesses versatile catalytic properties, displaying not only the ability to hydrolyze glycosidic linkages but also to synthesize furanobiosides in α-L-Araf and β-D-Galf series. H

Enzymatic synthesis of oligo-d-galactofuranosides and l-arabinofuranosides: From molecular dynamics to immunological assays

D-Galactofuranosyl-containing conjugates are ubiquitous in many pathogenic microorganisms, but completely absent from mammals. As they may constitute interesting pharmacophores, recent works have been dedicated to their preparation. Besides well-reported

Synthesis of pentose-containing disahharides using a thermostable α-L-arabinofuranosidase

To date, the enzymatically-catalysed synthesis of pentose-containing compounds has been limited to the production of oligo-β-(1->3)- and oligo-β-(1->4)-linked xylopyranosides. To our knowledge, no such syntheses have involved arabinofuranose or, indeed, a