Medicinal Chemistry, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3052, Australia.
Department of Microbiology, Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.
Biochem Soc Trans. 2020 Oct 30;48(5):2067-2078. doi: 10.1042/BST20200224.
Malaria continues to be a global health threat, affecting approximately 219 million people in 2018 alone. The recurrent development of resistance to existing antimalarials means that the design of new drug candidates must be carefully considered. Understanding of drug target mechanism can dramatically accelerate early-stage target-based development of novel antimalarials and allows for structural modifications even during late-stage preclinical development. Here, we have provided an overview of three promising antimalarial molecular targets, PfDHFR, PfDHODH and PfA-M1, and their associated inhibitors which demonstrate how mechanism can inform drug design and be effectively utilised to generate compounds with potent inhibitory activity.
疟疾仍然是一个全球性的健康威胁,仅在 2018 年就影响了约 2.19 亿人。现有抗疟药物的耐药性不断发展,这意味着必须仔细考虑新药物候选物的设计。对药物靶点机制的了解可以大大加速新型抗疟药物的早期基于靶点的开发,并允许在晚期临床前开发阶段进行结构修改。在这里,我们提供了三个有前途的抗疟分子靶点 PfDHFR、PfDHODH 和 PfA-M1 及其相关抑制剂的概述,展示了机制如何为药物设计提供信息,并有效地用于生成具有强大抑制活性的化合物。