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基于结构的神经氨酸酶抑制剂设计作为抗流感药物的最新进展。

Recent advances in the structure-based design of neuraminidase inhibitors as antiinfluenza agents.

机构信息

Department of Pharmacy, The First Affiliated Hospital of Medical College, Xi'an Jiaotong University, Xi'an, Shaanxi Province, 710061, PR China.

出版信息

Curr Med Chem. 2012;19(34):5885-94. doi: 10.2174/092986712804143358.

Abstract

Influenza is an infection of the upper respiratory tract caused by influenza virus. Neuraminidase (NA) plays an essential role in replication and infection of influenza virus. It is considered as a suitable target for antivirus agents development. Several potent NA inhibitors (NAIs) developed by using structure-based rational design have been widely used in clinic for treatment of influenza. However, the emergence of NA inhibitor-resistant virus mutations significantly limit their effectiveness. The molecular basis of virus resistance to NAIs has been a focus of intensive research. This review highlights recent progress in rational design and resistance mechanism of NAIs. We hope this review will be useful to not only researchers who are interested in developing novel NAIs but also clinical pharmacists.

摘要

流感是由流感病毒引起的上呼吸道感染。神经氨酸酶(NA)在流感病毒的复制和感染中起着至关重要的作用。它被认为是开发抗病毒药物的合适靶点。几种基于结构的合理设计开发的强效神经氨酸酶抑制剂(NAIs)已广泛用于临床治疗流感。然而,NAI 耐药病毒突变的出现显著限制了它们的有效性。病毒对 NAI 耐药的分子基础一直是密集研究的焦点。本综述重点介绍了 NAI 的合理设计和耐药机制的最新进展。我们希望本综述不仅对有兴趣开发新型 NAI 的研究人员有用,而且对临床药师也有用。

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