Literature DB >> 18049474

The design of drugs for HIV and HCV.

Erik De Clercq1.   

Abstract

Since the discovery of the human immunodeficiency virus (HIV) in 1983, dramatic progress has been made in the development of novel antiviral drugs. The HIV epidemic fuelled the development of new antiviral drug classes, which are now combined to provide highly active antiretroviral therapies. The need for the treatment of hepatitis C virus (HCV), which was discovered in 1989, has also provided considerable impetus for the development of new classes of antiviral drugs, and future treatment strategies for chronic HCV might involve combination regimens that are analogous to those currently used for HIV. By considering the drug targets in the different stages of the life cycle of these two viruses, this article presents aspects of the history, medicinal chemistry and mechanisms of action of approved and investigational drugs for HIV and HCV, and highlights general lessons learned from anti-HIV-drug design that could be applied to HCV.

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Year:  2007        PMID: 18049474     DOI: 10.1038/nrd2424

Source DB:  PubMed          Journal:  Nat Rev Drug Discov        ISSN: 1474-1776            Impact factor:   84.694


  89 in total

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4.  Solution structure of a hydrocarbon stapled peptide inhibitor in complex with monomeric C-terminal domain of HIV-1 capsid.

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5.  The HEPT Analogue WPR-6 Is Active against a Broad Spectrum of Nonnucleoside Reverse Transcriptase Drug-Resistant HIV-1 Strains of Different Serotypes.

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8.  Class III phosphatidylinositol 4-kinase alpha and beta are novel host factor regulators of hepatitis C virus replication.

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10.  Inhibition of HIV-1 entry by extracts derived from traditional Chinese medicinal herbal plants.

Authors:  In-Woo Park; Changri Han; Xiaoping Song; Linden A Green; Ting Wang; Ying Liu; Changchun Cen; Xinming Song; Biao Yang; Guangying Chen; Johnny J He
Journal:  BMC Complement Altern Med       Date:  2009-08-05       Impact factor: 3.659

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