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基于结构的药物发现方法;晶体学及其对抗寄生虫药物开发的影响。

A structure-based approach to drug discovery; crystallography and implications for the development of antiparasite drugs.

作者信息

Hunter W N

机构信息

Department of Biochemistry, University of Dundee, Scotland, UK.

出版信息

Parasitology. 1997;114 Suppl:S17-29.

PMID:9309766
Abstract

Advances in the life and physical sciences have enabled us to characterize the 3-dimensional structure and the biochemical or biological activity of both small and large molecules. The use of structural chemistry to assist understanding of biological activity provides information relevant to the design, development or identification of new pharmaceuticals. This structure based approach has become an important component of drug research and is in widespread use by the major pharmaceutical companies. A brief historical introduction, to convey how this area of science has reached the present stage, is given. The basis of the structural approach to understanding the chemistry of small and large molecule biological activity is outlined with an emphasis on the use of results derived from X-ray diffraction methods. Developments in other areas are discussed to emphasize the multidisciplinary nature of this research and the benefits of combining different methods. Examples of protein crystallographic studies in the area of molecular parasitology, some of which are directly relevant to antiparasite drug design, are presented. The characterization of the enzyme trypanothione reductase, a project which has benefited from many of the recent developments, is detailed. Future challenges and difficulties, both scientific and economic, are discussed.

摘要

生命科学和物理科学的进展使我们能够描述小分子和大分子的三维结构以及它们的生化或生物活性。利用结构化学来辅助理解生物活性,可为新药物的设计、开发或鉴定提供相关信息。这种基于结构的方法已成为药物研究的重要组成部分,并被各大制药公司广泛使用。本文给出了一个简短的历史介绍,以说明这一科学领域是如何发展到当前阶段的。概述了基于结构的方法来理解小分子和大分子生物活性化学的基础,重点是使用X射线衍射方法获得的结果。还讨论了其他领域的进展,以强调这项研究的多学科性质以及结合不同方法的益处。介绍了分子寄生虫学领域蛋白质晶体学研究的实例,其中一些与抗寄生虫药物设计直接相关。详细介绍了受益于近期许多进展的锥虫硫醇还原酶项目的表征。讨论了未来在科学和经济方面面临的挑战和困难。

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