Spiroindolone NITD609 is a novel antimalarial drug that targets the P-type ATPase PfATP4

被引:52
|
作者
Turner, Helen [1 ]
机构
[1] Open Univ, Dept Life Hlth & Chem Sci, Walton Hall, Milton Keynes MK7 6AA, Bucks, England
关键词
cipargamin; KAE609; malaria; NIDT609; PfATP4; Plasmodium; spiroindolone; NEXT-GENERATION ANTIMALARIAL; PLASMODIUM-FALCIPARUM; MALARIA PARASITE; KAE609; POTENT; MEDICINES; TRANSPORT;
D O I
10.4155/fmc.15.177
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Malaria is caused by the Plasmodium parasite and is a major health problem leading to many deaths worldwide. Lack of a vaccine and increasing drug resistance highlights the need for new antimalarial drugs with novel targets. Antiplasmodial activity of spiroindolones was discovered through whole-cell, phenotypic screening methods. Optimization of the lead spiroindolone improved both potency and pharmacokinetic properties leading to drug candidate NITD609 which has produced encouraging results in clinical trials. Spiroindolones inhibit PfATP4, a P-type Na+-ATPase in the plasma membrane of the parasite, causing a fatal disruption of its sodium homeostasis. Other diverse compounds from the Malaria Box appear to target PfATP4 warranting further research into its structure and binding with NITD609 and other potential antimalarial drugs.
引用
收藏
页码:227 / 238
页数:12
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