Synthesis of 2-(β-d-glucopyranosyl)-5-(substituted-amino)-1,3,4-oxa- and -thiadiazoles for the inhibition of glycogen phosphorylase
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference22 articles.
1. Prospects for Pharmacologic Inhibition of Hepatic Glucose Production
2. Intervention of Hepatic Glucose Production. Small Molecule Regulators of Potential Targets for Type 2 Diabetes Therapy
3. Chemistry and Biochemistry of Type 2 Diabetes
4. New Inhibitors of Glycogen Phosphorylase as Potential Antidiabetic Agents
5. Inhibition of Glycogen Phosphorylase in the Context of Type 2 Diabetes, with Focus on Recent Inhibitors Bound at the Active Site
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1. Efficient synthesis of novel 2-deoxy-C-nucleosides containing oxa and thiadiazole derivatives and their biological activity;Journal of Molecular Structure;2023-11
2. Comparative Study of the Synthetic Approaches and Biological Activities of the Bioisosteres of 1,3,4-Oxadiazoles and 1,3,4-Thiadiazoles over the Past Decade;Molecules;2022-04-22
3. N- and C-Glycopyranosyl heterocycles as glycogen phosphorylase inhibitors;Recent Trends in Carbohydrate Chemistry;2020
4. New syntheses towards C-glycosyl type glycomimetics;Pure and Applied Chemistry;2019-04-29
5. Addition of Organozinc Reagents to Glycopyranosyl Cyanides: Access to Keto Ester-C-glycosides or Unsaturated Acyl-C-glycosides;European Journal of Organic Chemistry;2018-04-17
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