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2000
Volume 7, Issue 6
  • ISSN: 0929-8673
  • E-ISSN: 1875-533X

Abstract

Rational drug design utilizing available X-ray crystal structures of sialic acid analogues bound to the active site of influenza virus neuraminidase has led to the discovery of a series of potent carbocyclic influenza neuraminidase inhibitors. From this series, GS 4104 (oseltamivir, TAMIFLU) has emerged as a promising antiviral for the treatment and prophylaxis of human influenza infection. This article will summarize the design, discovery, and development of oseltamivir as an oral therapeutic to treat influenza infection.

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/content/journals/cmc/10.2174/0929867003374886
2000-06-01
2025-05-07
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