Structure-Based Design of Nonpeptidic HIV Protease Inhibitors from a Cyclooctylpyranone Lead Structure-Reference-Cited by-同舟云学术

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Structure-Based Design of Nonpeptidic HIV Protease Inhibitors from a Cyclooctylpyranone Lead Structure

Published:1995-10 Issue:22 Volume:38 Page:4463-4473
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Romines Karen R.,Watenpaugh Keith D.,Howe W. Jeffrey,Tomich Paul K.,Lovasz Kristine D.,Morris Jeanette K.,Janakiraman Musiri N.,Lynn Janet C.,Horng Miao-Miao

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm00022a011

Cited by 39 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Quantitative structure-activity relationship (QSAR) models and their applicability domain analysis on HIV-1 protease inhibitors by machine learning methods;Chemometrics and Intelligent Laboratory Systems;2020-01

3. Studies on HIV-1 Protease and its Inhibitors;Viral Proteases and Their Inhibitors;2017

4. Therapeutic potential of coumarins as antiviral agents;European Journal of Medicinal Chemistry;2016-11

5. Exploring the Water-Binding Pocket of the Type II Dehydroquinase Enzyme in the Structure-Based Design of Inhibitors;Journal of Medicinal Chemistry;2014-04-15

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