95066-29-8Relevant academic research and scientific papers
Design Synthesis and Preliminary Evaluation of a Potent &α-Mannosidase Inhibitor: 1,4-Dideoxy-1,4-imino-D-mannitol
Fleet, George W. J.,Smith, Paul W.,Evans, Stephen V.,Fellows, Linda E.
, p. 1240 - 1241 (1984)
1,4-Dideoxy-1,4-imino-D-mannitol (1), synthesised from benzyl α-D-mannopyranoside, is a potent competitive inhibitor of the hydrolysis of p-nitrophenyl α-D-mannopyranoside catalysed by Jack Bean α-mannosidase (Canavalia ensiformis); this is the first repo
3, 5, and/or 6 substituted analogues of swainsonine processes for their preparation and their use as therapeutic agents
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, (2008/06/13)
The invention relates to novel 3, 5, and/or 6 swainsonine analogues, processes for their preparation and their use as therapeutic agents. The invention also relates to pharmaceutical compositions containing the compounds and their use as therapeutics.
SYNTHESIS OF THE α-MANNOSIDASE INHIBITORS SWAINSONINE AND 1,4-DIDEOXY-1,4-IMINO-D-MANNITOL FROM MANNOSE
Bashyal, Bharat P.,Fleet, George W. J.,Gough, Max J.,Smith, Paul W.
, p. 3083 - 3094 (2007/10/02)
4-azido-4-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside is a key intermediate in the syntheses of the α-mannosidase inhibitors, swainsonine and 1,4-dideoxy-1,4-imino-D-mannitol, and of the α-galactosidase inhibitor 1,4-dideoxy-1,4-imino-D-lyxitol, from mannose.
