Synthesis of N-Glucopyranosidic Derivatives as Potential Inhibitors that Bind at the Catalytic Site of Glycogen Phosphorylase
Author:
Publisher
Bentham Science Publishers Ltd.
Subject
Drug Discovery,Pharmacology,General Medicine
Cited by 27 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Urea‐catalyzed N‐Glycosylation of Amides/Azacycles with Glycosyl Halides;Chemistry – An Asian Journal;2023-11-02
2. A glucose-based molecular rotor inhibitor of glycogen phosphorylase as a probe of cellular enzymatic function;Organic & Biomolecular Chemistry;2022
3. Synthesis, Kinetic and Conformational Studies of 2-Substituted-5-(β-d-glucopyranosyl)-pyrimidin-4-ones as Potential Inhibitors of Glycogen Phosphorylase;Molecules;2020-11-22
4. The architecture of hydrogen and sulfur σ-hole interactions explain differences in the inhibitory potency of C-β-d-glucopyranosyl thiazoles, imidazoles and an N-β-d glucopyranosyl tetrazole for human liver glycogen phosphorylase and offer new insights to structure-based design;Bioorganic & Medicinal Chemistry;2020-01
5. N- and C-Glycopyranosyl heterocycles as glycogen phosphorylase inhibitors;Recent Trends in Carbohydrate Chemistry;2020
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