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恶性疟原虫和间日疟原虫抗疟耐药性的分子与生物学方面

Molecular and biological aspects of antimalarial resistance in Plasmodium falciparum and Plasmodium vivax.

作者信息

Bustamante Carolina, Batista Camila Nunes, Zalis Mariano

机构信息

Laboratório de Infectologia e Parasitologia Molecular, Hospital Universitário Clementino Fraga Filho, Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Ilha do Fundão, RJ, Brasil.

出版信息

Curr Drug Targets. 2009 Mar;10(3):279-90. doi: 10.2174/138945009787581131.

Abstract

The development of antimalarial drugs involving novel mechanisms of action is of imminent importance. Several potential drug candidates of synthetic and natural origin as well as their combination therapies are currently being evaluated for their efficacy against drug-resistant strains of the parasite. Various plasmodial targets/pathways, such as the Purine salvage pathway, Pyrimidine biosynthesis pathway and also the processes in the apicoplast, have been identified and are being utilized for the discovery and development of novel antimalarial therapies. This article provides an overview of the latest developments in terms of cell and molecular biology that will improve the knowledge related to drug-resistant malaria and to new molecular targets.

摘要

开发具有新型作用机制的抗疟药物迫在眉睫。目前正在评估几种合成和天然来源的潜在候选药物及其联合疗法对寄生虫耐药菌株的疗效。已经确定了各种疟原虫靶点/途径,如嘌呤补救途径、嘧啶生物合成途径以及顶质体中的过程,并正在将其用于发现和开发新型抗疟疗法。本文概述了细胞和分子生物学方面的最新进展,这些进展将增进对耐药疟疾和新分子靶点的了解。

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