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针对黄病毒的新型抗病毒药物的研发。

Development of novel antivirals against flaviviruses.

作者信息

Patkar Chinmay G, Kuhn Richard J

机构信息

Department of Biological Sciences, Purdue University, 915 West State Street, West Lafayette, IN 47907-2054, USA.

出版信息

Novartis Found Symp. 2006;277:41-52; discussion 52-6, 71-3, 251-3.

Abstract

Dengue virus is responsible for a significant amount of human disease in predominantly tropical areas of the world. Much effort has focused on the development of vaccines against the four serotypes of dengue, and within the next few years a vaccine is anticipated. Less progress has been made at developing antivirals that might reduce disease severity. Recent advances in the structural biology of dengue virus and other flaviviruses have opened new possibilities for the rational design of small molecule inhibitors of virus replication. This chapter describes the structural attributes of the dengue virion and how knowledge of its structure, assembly, and entry mechanisms are guiding new strategies toward the development of compounds that will interfere with the viral replication process.

摘要

登革病毒在世界主要热带地区引发了大量人类疾病。人们致力于研发针对登革热四种血清型的疫苗,预计未来几年将会有疫苗问世。在开发可能降低疾病严重程度的抗病毒药物方面进展较小。登革病毒及其他黄病毒结构生物学的最新进展为合理设计病毒复制小分子抑制剂开辟了新的可能性。本章描述了登革病毒粒子的结构特征,以及对其结构、组装和进入机制的了解如何指导开发干扰病毒复制过程的化合物的新策略。

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