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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 [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Schalli Michael
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Abstract:
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.

Find related publications in this database (Keywords)
Carbohydrates
Conformation
Enzymes
-Glucosidase ligands
Iminoxylitol
-Glucocerebrosidase
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