Anti-HIV nucleosides : past, present and future

Bibliographic Information

Anti-HIV nucleosides : past, present and future

[edited by] Hiroaki Mitsuya

(Medical intelligence unit)

Springer , R.G. Landes, c1997

  • :international
  • :US and Canada

Available at  / 3 libraries

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Includes bibliographical references and index

Description and Table of Contents

Description

In 1985, a broad family of dideoxynucleoside reverse transcriptase inhibitors were identified to be active against a divergent range of HIV in vitro. Three such drugs - AZT, ddC and ddI - had become prescription drugs by 1991. More recently, d4t and 3TC have been added to this nucleoside armamentarium. Indeed, despite their side-effects, insufficient antiviral activity and the propensity of HIV-1 to develop drug resistance, anti-HIV nucleosides have brought about substantial clinical benefits to HIV-1 infected individuals since the mid-1980s. Even with the development of new modalities of AIDS therapy, anti-HIV nucleosides will continue to play a major role in the therapy of HIV-1 infection. This volume discusses the development, rationale, present status, and the future of the use of anti-HIV nucleosides. Standing orders placed before December 31st, 1996 will receive a 10 per cent reduction off the list price of all volumes published with the series between the order date and December 31st, 1997. This offer is on a firm order basis only.

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