Structure-Based Design and Synthesis of Substituted 2-Butanols as Nonpeptidic Inhibitors of HIV Protease: Secondary Amide Series
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 39 (14) , 2781-2794
- https://doi.org/10.1021/jm960093o
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Bis Tertiary Amide Inhibitors of the HIV-1 Protease Generated via Protein Structure-Based Iterative DesignJournal of Medicinal Chemistry, 1996
- Protein structure-based design of potent orally bioavailable, nonpeptide inhibitors of human immunodeficiency virus protease.Proceedings of the National Academy of Sciences, 1995
- HIV Protease as an Inhibitor Target for the Treatment of AIDSPublished by Elsevier ,1994
- Climate Extravaganza BombsScience, 1990
- Insect sex pheromones. Stereospecific synthesis of (E)-13,13-dimethyl-11-tetradecen-1-ol acetate via a thiophenol-mediated olefin inversionThe Journal of Organic Chemistry, 1986
- Synthesis of arylacetylenes by the sodium hydride catalyzed cleavage of 4-aryl-2-methyl-3-butyn-2-olsThe Journal of Organic Chemistry, 1985