| Literature DB >> 10702632 |
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.Entities:
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Year: 2000 PMID: 10702632 DOI: 10.2174/0929867003374886
Source DB: PubMed Journal: Curr Med Chem ISSN: 0929-8673 Impact factor: 4.530