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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Schalli, M; Wolfsgruber, A; Gonzalez Santana, A; Tysoe, C; Fischer, R; Stütz, AE; Thonhofer, M; Withers, SG.
C-5a-substituted validamine type glycosidase inhibitors.
Carbohydr Res. 2017; 440-441(15): 1-9. Doi: 10.1016/j.carres.2017.01.006
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Führende Autor*innen der Med Uni Graz: Schalli Michael
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Abstract:: A series of N-alkyl derivatives of the D-galactosidase inhibitor 1,4-di-epi-validamine featuring lipophilic substituents at position C-5a was prepared and screened for their glycosidase inhibitory properties. Products turned out selective for β-galactosidases as well as β-glucosidases. Copyright © 2017 Elsevier Ltd. All rights reserved.
Find related publications in this database (using NLM MeSH Indexing): Agrobacterium - chemistry; Agrobacterium - enzymology; Animals -; Bacterial Proteins - antagonists & inhibitors; Bacterial Proteins - chemistry; Carbohydrate Conformation -; Cattle -; Enzyme Inhibitors - chemical synthesis; Enzyme Inhibitors - chemistry; Escherichia coli - chemistry; Escherichia coli - enzymology; Fungal Proteins - antagonists & inhibitors; Fungal Proteins - chemistry; Hydrophobic and Hydrophilic Interactions -; Inositol - analogs & derivatives; Inositol - chemical synthesis; Inositol - chemistry; Kinetics -; Saccharomyces cerevisiae - chemistry; Saccharomyces cerevisiae - enzymology; beta-Galactosidase - antagonists & inhibitors; beta-Galactosidase - chemistry; beta-Glucosidase - antagonists & inhibitors; beta-Glucosidase - chemistry
Find related publications in this database (Keywords): Aminocyclitol; Carbasugar; Glycosidase inhibitor

Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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