Chiral resolution, determination of absolute configuration, and biological evaluation of (1,2-benzothiazin-4-yl)acetic acid enantiomers as aldose reductase inhibitors-Reference-Cited by-同舟云学术

Chiral resolution, determination of absolute configuration, and biological evaluation of (1,2-benzothiazin-4-yl)acetic acid enantiomers as aldose reductase inhibitors

Published:2015-08-27 Issue:5 Volume:30 Page:846-851
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Hao Xin¹,Qin Xiangyu¹,Hussain Saghir¹,Parveen Shagufta¹,Zhang Wei¹,Fu Fengyan¹,Ma Bing¹,Zhu Changjin¹

Affiliation:

1. Department of Applied Chemistry, Beijing Institute of Technology, Beijing, China

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.3109/14756366.2014.961447

Reference26 articles.

1. Formation of Polyols by the Lens of the Rat with ‘Sugar’ Cataract

2. Sorbitol Pathway: Presence in Nerve and Cord with Substrate Accumulation in Diabetes

3. Genetic Analysis of Aldose Reductase in Diabetic Complications

4. The role of aldose reductase gene in the susceptibility to diabetic nephropathy in Type II (non-insulin-dependent) diabetes mellitus (Short Communication)

5. A novel polymorphism in the aldose reductase gene promoter region is strongly associated with diabetic retinopathy in adolescents with type 1 diabetes.

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