Medicinal Chemistry, Monash Institute of Pharmaceutical Sciences, Monash University , Parkville, Victoria 3052, Australia.
J Med Chem. 2014 Nov 13;57(21):9168-83. doi: 10.1021/jm501323a. Epub 2014 Oct 24.
Plasmodium parasites, the causative agents of malaria, have developed resistance to most of our current antimalarial therapies, including artemisinin combination therapies which are widely described as our last line of defense. Antimalarial agents with a novel mode of action are urgently required. Two Plasmodium falciparum aminopeptidases, PfA-M1 and PfA-M17, play crucial roles in the erythrocytic stage of infection and have been validated as potential antimalarial targets. Using compound-bound crystal structures of both enzymes, we have used a structure-guided approach to develop a novel series of inhibitors capable of potent inhibition of both PfA-M1 and PfA-M17 activity and parasite growth in culture. Herein we describe the design, synthesis, and evaluation of a series of hydroxamic acid-based inhibitors and demonstrate the compounds to be exciting new leads for the development of novel antimalarial therapeutics.
疟原虫寄生虫是疟疾的病原体,已经对我们目前的大多数抗疟疗法产生了耐药性,包括被广泛描述为我们最后一道防线的青蒿素联合疗法。迫切需要具有新作用模式的抗疟药物。两种恶性疟原虫氨肽酶,PfA-M1 和 PfA-M17,在感染的红细胞阶段发挥关键作用,并已被验证为潜在的抗疟靶点。利用两种酶的结合化合物晶体结构,我们采用了一种基于结构的方法来开发一系列新型抑制剂,这些抑制剂能够强烈抑制 PfA-M1 和 PfA-M17 的活性以及培养中的寄生虫生长。本文描述了一系列基于羟肟酸的抑制剂的设计、合成和评价,并证明这些化合物是开发新型抗疟治疗药物的令人兴奋的新先导物。