Discovery of New Selective Human Aldose Reductase Inhibitors through Virtual Screening Multiple Binding Pocket Conformations-Reference-Cited by-同舟云学术

Discovery of New Selective Human Aldose Reductase Inhibitors through Virtual Screening Multiple Binding Pocket Conformations

Published:2013-08-26 Issue:9 Volume:53 Page:2409-2422
ISSN:1549-9596
Container-title:Journal of Chemical Information and Modeling
language:en
Short-container-title:J. Chem. Inf. Model.

Author:

Wang Ling¹,Gu Qiong¹,Zheng Xuehua¹,Ye Jiming²,Liu Zhihong¹,Li Jiabo³,Hu Xiaopeng¹,Hagler Arnold⁴⁵,Xu Jun¹

Affiliation:

1. Research Center for Drug Discovery & Institute of Human Virology, School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China

2. Molecular Pharmacology for Diabetes Group, Health Innovations Research Institute and School of Health Sciences, RMIT University, Melbourne, VIC 3083, Australia

3. Accelrys Inc., 10188 Telesis Court, San Diego, California 92121, United States

4. Department of Chemistry, University of Massachusetts, 701 Lederle Graduate Research Tower, 710 North Pleasant Street, Amherst, Massachusetts 01003-9336, United States

5. Shifa Biomedical, 1 Great Valley Parkway, Suite 8, Malvern, Pennsylvania 19355, United States

Publisher

American Chemical Society (ACS)

Subject

Library and Information Sciences,Computer Science Applications,General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ci400322j

Reference69 articles.

1. Structure-Based Optimization of Aldose Reductase Inhibitors Originating from Virtual Screening

2. Biochemistry and molecular cell biology of diabetic complications

3. Aldose reductase inhibitors: a potential new class of agents for the pharmacological control of certain diabetic complications

4. The involvement of aldose reductase in diabetic complications

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