A series of pyrido[2,3-b]pyrazin-3(4H)-one derivatives as aldose reductase inhibitors with antioxidant activity-Reference-Cited by-同舟云学术

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A series of pyrido[2,3-b]pyrazin-3(4H)-one derivatives as aldose reductase inhibitors with antioxidant activity

Published:2016-10 Issue: Volume:121 Page:308-317
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Han Zhongfei,Hao Xin,Ma Bing,Zhu Changjin

Funder

National Natural Science Foundation of China

Doctoral Program of Higher Education of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference45 articles.

1. Acetic acid derivatives of 3,4-Dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide as a novel class of potent aldose reductase inhibitors;Chen;J. Med. Chem.,2010

2. Biochemistry and molecular cell biology of diabetic complications;Brownlee;Nature,2001

3. Chalcones and their therapeutic targets for the management of diabetes: structural and pharmacological perspectives;Mahapatra;Eur. J. Med. Chem.,2015

4. IDF Diabetes Atlas;Aguiree,2013

5. Aromatic heterobicyclics-based design of aldose reductase inhibitors as drug candidates for the treatment of diabetic complications;Han;Adv. Tech. Biol. Med.,2015

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1. Synthesis of novel 7-substituted pyrido[3,2-b]pyrazin-3(4H)-one derivatives via Suzuki-Miyaura cross-coupling reaction;Journal of the Indian Chemical Society;2024-07

2. Discovery of the Quinoxalinone–B(C₆F₅)₃·H₂O Combo as a Photocatalyst by Acidochromism Strategy: Aerobic Oxidation of Alcohol, Alkene, and Thiols;Organic Letters;2023-07-20

3. Design and synthesis of novel quinazolin‐4(1H)‐one derivatives as potent and selective inhibitors targeting AKR1B1;Archiv der Pharmazie;2023-01-27

4. Design of Improved Antidiabetic Drugs: A Journey from Single to Multitarget Agents;ChemMedChem;2022-10-26

5. Strategies in synthetic design and structure–activity relationship studies of novel heterocyclic scaffolds as aldose reductase‐2 inhibitors;Archiv der Pharmazie;2022-09-20

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