Synthesis of C2-symmetric HIV-protease inhibitors with sulfur-containing central units
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Active human immunodeficiency virus protease is required for viral infectivity.
2. HTLV-III gag Protein Is Processed in Yeast Cells by the Virus pol -Protease
3. Peptide substrates and inhibitors of the HIV-1 protease
4. A Synthetic HIV-1 Protease Inhibitor with Antiviral Activity Arrests HIV-Like Particle Maturation
5. Rational Design of Peptide-Based HIV Proteinase Inhibitors
Cited by 14 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
1. ChemInform Abstract: Synthesis of C2-Symmetric HIV-Protease Inhibitors with Sulfur- Containing Central Units.;ChemInform;2010-08-20
2. Discovery of potent HIV-1 protease inhibitors incorporating sulfoximine functionality;Bioorganic & Medicinal Chemistry Letters;2007-10
3. Oxidation of sulfides to sulfoxides. Part 1: Oxidation using halogen derivatives;Tetrahedron;2005-02
4. Synthesis and Biological Activity of Hydroxamic Acid-Derived Vasopeptidase Inhibitor Analogues;Organic Letters;2002-05-14
5. A convergent, stereocontrolled synthesis of C2-symmetrical and pseudosymmetrical sulfur-tethered bis(amino alcohols);Tetrahedron Letters;1999-05
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