Positional isomers of thioxylobiose, their synthesis and inducing ability for d-xylan-degrading enzymes in the yeast cryptococcus albidus☆
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Synthesis, in vitro antimicrobial and in vivo antitumor evaluation of novel pyrimidoquinolines and its nucleoside derivatives
2011, European Journal of Medicinal ChemistryCitation Excerpt :N-Glycosides have received considerable attention, because they are widely employed as biological inhibitors [19–23], inducers [24] and ligands [25–27] for affinity chromatography of carbohydrate-processing enzymes and proteins. Moreover, they are promising candidates in synthetic carbohydrate chemistry as convenient and versatile glycosyl donors [28]. Among these glycosyl donors are the N-glycosyl heterocycles that are sufficiently stable under a variety of reaction conditions and have the ability to be readily converted into a variety of other functionalities.
Synthesis and antitumor activity of new dihydropyridine thioglycosides and their corresponding dehydrogenated forms
2010, European Journal of Medicinal ChemistryCitation Excerpt :On the other hand, thioglycosides have received considerable attention, because they are widely employed as biological inhibitors [19–22], inducers [23] and ligands [24–26] for affinity chromatography for carbohydrate processing-enzymes and proteins. Thiopyridyl glycosides were extensively studied because of their potential activity as glycosyl donors [27]. A number of novel synthesized functionalized pyridinethione glycosides have been shown to exhibit antagonistic activity against human carcinoma cells and HIV-virus [28–30].
Synthesis of pentopyranosyl-containing thiodisaccharides. Inhibitory activity against β-glycosidases
2009, Bioorganic and Medicinal ChemistryXylanases, xylanase families and extremophilic xylanases
2005, FEMS Microbiology Reviews
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Stereoselective Thioglycoses Synthesis, Part XIV. For Part XII, see ref. 1; for Part XIII, see ref. 2.
- 1
Equipe CNRS, SDI 5509.