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Zoidl, M; Wolfsgruber, A; Schalli, M; Nasseri, SA; Weber, P; Stütz, AE; Withers, SG; Wrodnigg, TM.
Synthesis of modified 1,5-imino-d-xylitols as ligands for lysosomal β-glucocerebrosidase.
Monatsh Chem. 2019; 150(5): 831-842.
Doi: 10.1007/s00706-019-02427-1
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- Co-Autor*innen der Med Uni Graz
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Schalli Michael
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- Abstract:
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Modified 1,5-dideoxy-1,5-imino-d-xylitol analogues with different substitution patterns involving position C-1 and/or the ring nitrogen were prepared, which were designed to serve as precursors for the preparation of iminoxylitol-based ligands and tools for the elucidation and modulation of human lysosomal β-glucocerebrosidase. Biological evaluation of the synthesized glycomimetics with a series of glycoside hydrolases revealed that these substitution patterns elicit excellent β-glucosidase selectivities.
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Carbohydrates
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Conformation
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Enzymes
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-Glucosidase ligands
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Iminoxylitol
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-Glucocerebrosidase