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流感病毒神经氨酸酶芳香族抑制剂的设计

Design of aromatic inhibitors of influenza virus neuraminidase.

作者信息

Luo M, Air G M, Brouillette W J

机构信息

Center for Macromolecular Crystallography, Department of Microbiology, University of Alabama at Birmingham, 35294, USA.

出版信息

J Infect Dis. 1997 Aug;176 Suppl 1:S62-5. doi: 10.1086/514178.

Abstract

Structure-based drug design, a terminology used to describe rational drug design by complementing the structure, spatially and chemically, of the target macromolecule, is rapidly developing as one of the innovative approaches to drug discovery. A growing volume of protein structure data and new techniques of protein structure determination make this all possible. The method of structure-based drug design and a specific example of the design of influenza virus neuraminidase is briefly presented. A whole new class of influenza virus neuraminidase inhibitors has been designed that can potentially be developed as antiinfluenza drugs.

摘要

基于结构的药物设计是一种通过在空间和化学上补充目标大分子的结构来描述合理药物设计的术语,作为药物发现的创新方法之一正在迅速发展。越来越多的蛋白质结构数据和新的蛋白质结构测定技术使这一切成为可能。本文简要介绍了基于结构的药物设计方法以及流感病毒神经氨酸酶设计的一个具体实例。已经设计出了全新一类的流感病毒神经氨酸酶抑制剂,它们有可能被开发成抗流感药物。

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