Structure-Based Design and Synthesis of Substituted 2-Butanols as Nonpeptidic Inhibitors of HIV Protease: Secondary Amide Series
Author:
Affiliation:
1. Agouron Pharmaceuticals, Inc., 3565 General Atomics Court, San Diego, California 92121
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm960093o
Reference11 articles.
1. Darke, P. L.; Huff, J. R. In HIV Protease as an Inhibitor Target for the Treatment of Aids. InAdvances in Pharmacology; August, J. T., Ander, M. W., Murad, F., Eds.; Academic Press: San Diego, 1994; Vol. 25, pp 399−454 and references cited therein.
2. Protein structure-based design of potent orally bioavailable, nonpeptide inhibitors of human immunodeficiency virus protease.
3. Climate Extravaganza Bombs
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