Chapter 15. Antiviral Agents
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Elsevier
Reference76 articles.
1. Crystal structure of a tethered dimer of HIV-1 proteinase complexed with an inhibitor
2. The activity of the protease of human immunodeficiency virus type 1 is initiated at the membrane of infected cells before the release of viral proteins and is required for release to occur with maximum efficiency.
3. HIV protease inhibitors: effects on viral maturation and physiologic function in macrophages
4. Antiviral activity of human immunodeficiency virus type 1 protease inhibitors in a single cycle of infection: evidence for a role of protease in the early phase
5. A possible regulation of negative factor (Nef) activity of human immunodeficiency virus type 1 by the viral protease
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1. Modeling of novel HIV-1 protease inhibitors incorporating N-Aryl-oxazolidinone-5-carboxamides as P2 ligands using quantum chemical and topological finger print descriptors;Medicinal Chemistry Research;2010-09-06
2. Quantitative Structure-Activity Relationship of some HIV-1 Protease Inhibitors: A Fujita-Ban Type Analysis;Journal of Enzyme Inhibition;2001-01
3. Efficient hydrolysis of β-aminosulfamic acids using a Lewis acid and a thiol for the synthesis of 2,3-diaminopropanoate derivatives;Tetrahedron Letters;1998-07
4. Quantitative Structure-Activity Relationship Studies on Cyclic Urea-Based HIV Protease Inhibitors;Journal of Enzyme Inhibition;1998-01
5. The discovery, characterization and crystallographically determined binding mode of an FMOC-containing inhibitor of HIV-1 protease;Bioorganic & Medicinal Chemistry;1997-07
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