Synthesis and biological evaluation of novel 1,2,4-triazine derivatives bearing carbazole moiety as potent α-glucosidase inhibitors-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of novel 1,2,4-triazine derivatives bearing carbazole moiety as potent α-glucosidase inhibitors

Published:2016-06 Issue:12 Volume:26 Page:2806-2809
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Wang Guangcheng,Wang Jing,He Dianxiong,Li Xin,Li Juan,Peng Zhiyun

Funder

Hunan Provincial Natural Science Foundation of China

Scientific Research Fund of Hunan Provincial Education Department

Jishou University

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference32 articles.

1. Hyperglycemic Crises in Adult Patients With Diabetes

2. Epidemiology of Diabetes and Diabetes-Related Complications

3. Postprandial hyperglycaemia and α-glucosidase inhibitors

4. Effect of the postprandial state on nontraditional risk factors

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1. Synthesis of furo[2,3-c]carbazoles as potent α -glucosidase and α -amylase inhibitors;Synthetic Communications;2024-09-11

2. Recent Developments in 1,2,3‐Triazole Based α‐Glucosidase Inhibitors: Design Strategies, Structure‐Activity Relationship and Mechanistic Insights;Chemistry & Biodiversity;2024-08-22

3. Diverse pharmacological actions of potential carbazole derivatives by influencing various pathways of molecular signaling;Future Journal of Pharmaceutical Sciences;2024-06-17

4. Recyclable Palladium-Catalyzed Carbonylative Coupling of Aryl Halides and Organoaluminum Compounds with tert-Butyl Isocyanide as CO Equivalent Leading to 1,2-Diketones;Synthesis;2024-06-03

5. A Review on the Development of Novel Heterocycles as α-Glucosidase Inhibitors for the Treatment of Type-2 Diabetes Mellitus;Medicinal Chemistry;2024-06

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