The war against influenza: discovery and development of sialidase inhibitors

被引:539
作者
von Itzstein, Mark [1 ]
机构
[1] Griffith Univ, Inst Glycom, Nathan, Qld 4111, Australia
基金
澳大利亚研究理事会;
关键词
D O I
10.1038/nrd2400
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The threat of a major human influenza pandemic, in particular from highly aggressive strains such as avian H5N1, has emphasized the need for therapeutic strategies to combat these pathogens. At present, two inhibitors of sialidase (also known as neuraminidase), a viral enzyme that has a key role in the life cycle of influenza viruses, would be the mainstay of pharmacological strategies in the event of such a pandemic. This article provides a historical perspective on the discovery and development of these drugs - zanamivir and oseltamivir - and highlights the value of structure-based drug design in this process.
引用
收藏
页码:967 / 974
页数:8
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