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从青蒿素衍生物的机制研究到新型模块化抗疟药物

From mechanistic studies on artemisinin derivatives to new modular antimalarial drugs.

作者信息

Robert Anne, Dechy-Cabaret Odile, Cazelles Jérôme, Meunier Bernard

机构信息

Laboratoire de Chimie de Coordination du CNRS, 205 route de Narbonne, 31077 Toulouse Cedex 4, France.

出版信息

Acc Chem Res. 2002 Mar;35(3):167-74. doi: 10.1021/ar990164o.

Abstract

In the first part of this account, the antimalarial drug artemisinin is presented, and the current hypotheses on the mechanism of action of this endoperoxide-based drug are reviewed. The alkylating ability of artemisinin and synthetic analogues toward heme related to their antimalarial efficacy are underlined. Some possible ways for discovery of new drugs, especially the design of trioxaquines, new active molecules recently patented that have been prepared by covalent attachment of a trioxane residue having alkylating ability to a quinoline moiety known to easily penetrate within infected erythrocytes, are presented.

摘要

在本报告的第一部分,介绍了抗疟药物青蒿素,并综述了关于这种过氧化物类药物作用机制的当前假说。强调了青蒿素及其合成类似物对与抗疟功效相关的血红素的烷基化能力。还介绍了一些发现新药的可能途径,特别是三氧喹啉的设计,三氧喹啉是最近获得专利的新型活性分子,它是通过将具有烷基化能力的三恶烷残基共价连接到已知能轻易穿透受感染红细胞的喹啉部分而制备的。

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