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抗疟药物发现:从奎宁到最近最有前途的临床候选药物。

Antimalarial Drug Discovery: From Quinine to the Most Recent Promising Clinical Drug Candidates.

机构信息

AGIR UR4294, UFR de Pharmacie, Université de Picardie Jules Verne, Amiens, France.

LBHE UR2465, Université d'Artois, Lens, France.

出版信息

Curr Med Chem. 2022;29(19):3326-3365. doi: 10.2174/0929867328666210803152419.

Abstract

Malaria is a tropical threatening disease caused by Plasmodium parasites, resulting in 409,000 deaths in 2019. The delay of mortality and morbidity has been compounded by the widespread of drug resistant parasites from Southeast Asia since two decades. The emergence of artemisinin-resistant Plasmodium in Africa, where most cases are accounted, highlights the urgent need for new medicines. In this effort, the World Health Organization and Medicines for Malaria Venture joined to define clear goals for novel therapies and characterized the target candidate profile. This ongoing search for new treatments is based on imperative labor in medicinal chemistry which is summarized here with particular attention to hit-to-lead optimizations, key properties, and modes of action of these novel antimalarial drugs. This review, after presenting the current antimalarial chemotherapy, from quinine to the latest marketed drugs, focuses in particular on recent advances of the most promising antimalarial candidates in clinical and preclinical phases.

摘要

疟疾是一种热带传染病,由疟原虫引起,2019 年导致 40.9 万人死亡。由于二十年来东南亚耐药寄生虫的广泛传播,死亡率和发病率的延迟更加严重。在非洲,大多数病例都是由青蒿素耐药疟原虫引起的,这突显了急需新药物的紧迫性。在这方面的努力中,世界卫生组织和疟疾药物基金会共同为新疗法制定了明确的目标,并对目标候选物特征进行了描述。目前正在寻找新的治疗方法,这是基于药物化学方面的必要工作,本文特别关注了这些新型抗疟药物的命中到先导优化、关键特性和作用模式。本文在介绍了从奎宁到最新上市药物的当前抗疟化疗方法后,特别关注了临床和临床前阶段最有前途的抗疟候选药物的最新进展。

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