CDT-Africa, Addis Ababa University, Addis Ababa, Ethiopia.
Department of Pharmacology and Clinical Pharmacy, Addis Ababa University, Addis Ababa, Ethiopia.
Drug Des Devel Ther. 2020 Nov 11;14:4855-4867. doi: 10.2147/DDDT.S278588. eCollection 2020.
Malaria remains a global public health problem due to the uphill fight against the causative parasites that are relentless in developing resistance. Indole-based antiplasmodial compounds are endowed with multiple modes of action, of which inhibition of hemozoin formation is the major mechanism of action reported for compounds such as cryptolepine, flinderoles, and isosungucine. Indole-based compounds exert their potent activity against chloroquine-resistant strains by inhibiting hemozoin formation in a mode of action different from that of chloroquine or through a novel mechanism of action. For example, dysregulating the sodium and osmotic homeostasis of through inhibition of PfATP4 is the novel mechanism of cipargamin. The potential of developing multi-targeted compounds through molecular hybridization ensures the existence of indole-based compounds in the antimalarial pipeline.
疟疾仍然是一个全球性的公共卫生问题,因为要对抗那些不断产生抗药性的致病寄生虫还有很长的路要走。基于吲哚的抗疟化合物具有多种作用模式,其中抑制亚铁血红素的形成是隐丹参酮、弗林德罗林和异松虫草素等化合物的主要作用机制。基于吲哚的化合物通过抑制亚铁血红素的形成来发挥其对氯喹耐药株的强大活性,其作用模式与氯喹不同,或者通过一种新的作用机制。例如,通过抑制 PfATP4 来扰乱 的钠和渗透稳态是西帕氨基醇的新作用机制。通过分子杂交开发多靶点化合物的潜力确保了基于吲哚的化合物在抗疟药物研发中发挥作用。