二氢月桂酸脱氢酶
恶性疟原虫
疟疾
药物发现
嘧啶代谢
抗疟药
药理学
生物
酶
抗寄生虫药
生物化学
化学
免疫学
嘌呤
作者
Vivek K. Vyas,Tanvi Shukla,Manmohan Sharma
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2023-07-01
卷期号:15 (14): 1295-1321
标识
DOI:10.4155/fmc-2023-0113
摘要
Malaria is a severe human disease and a global health problem because of drug-resistant strains. Drugs reported to prevent the growth of Plasmodium parasites target various phases of the parasites' life cycle. Antimalarial drugs can inhibit key enzymes that are responsible for the cellular growth and development of parasites. Plasmodium falciparum dihydroorotate dehydrogenase is one such enzyme that is necessary for de novo pyrimidine biosynthesis. This review focuses on various medicinal chemistry approaches used for the discovery and identification of selective P. falciparum dihydroorotate dehydrogenase inhibitors as antimalarial agents. This comprehensive review discusses recent advances in the selective therapeutic activity of distinct chemical classes of compounds as P. falciparum dihydroorotate dehydrogenase inhibitors and antimalarial drugs.
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