Looking glass inhibitors: efficient synthesis and biological evaluation of D-deoxyfuconojirimycin.
1,6-Dideoxygalactostatin, the mirror image of 1-deoxy-L-fuconojirimycin, was efficiently prepared from 2,3-O-isopropylidene-L-lyxonolactone in four steps and evaluated as a glycosidase inhibitor.
Päätekijät: | Blériot, Y, Gretzke, D, Krülle, T, Butters, T, Dwek, R, Nash, R, Asano, N, Fleet, G |
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Aineistotyyppi: | Journal article |
Kieli: | English |
Julkaistu: |
2005
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Samankaltaisia teoksia
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Looking glass inhibitors: Efficient synthesis and biological evaluation of D-deoxyfuconojirimycin
Tekijä: Blériot, Y, et al.
Julkaistu: (2005) -
Looking glass inhibitors: L-DMDP, a more potent and specific inhibitor of α-glucosidases than the enantiomeric natural product DMDP
Tekijä: Yu, C, et al.
Julkaistu: (2004) -
Looking glass inhibitors: L-DMDP, a more potent and specific inhibitor of alpha-glucosidases than the enantiomeric natural product DMDP.
Tekijä: Yu, C, et al.
Julkaistu: (2004) -
Inhibition of alpha-L-fucosidase by derivatives of deoxyfuconojirimycin and deoxymannojirimycin.
Tekijä: Winchester, B, et al.
Julkaistu: (1990) -
SHORT EFFICIENT SYNTHESIS OF THE ALPHA-L-FUCOSIDASE INHIBITOR, DEOXYFUCONOJIRIMYCIN [1,5-DIDEOXY-1,5-IMINO-L-FUCITOL] FROM D-LYXONOLACTONE
Tekijä: Fleet, G, et al.
Julkaistu: (1989)