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发现二氢乳清酸脱氢酶抑制剂作为抗疟药物的药物化学方法。

Medicinal chemistry approaches for the discovery of dihydroorotate dehydrogenase inhibitors as antimalarial agents.

作者信息

Vyas Vivek K, Shukla Tanvi, Sharma Manmohan

机构信息

Department of Pharmaceutical Chemistry, Institute of Pharmacy, Nirma University, Ahmedabad, Gujarat, 382481, India.

出版信息

Future Med Chem. 2023 Jul;15(14):1295-1321. doi: 10.4155/fmc-2023-0113. Epub 2023 Aug 8.

Abstract

Malaria is a severe human disease and a global health problem because of drug-resistant strains. Drugs reported to prevent the growth of 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. dihydroorotate dehydrogenase is one such enzyme that is necessary for pyrimidine biosynthesis. This review focuses on various medicinal chemistry approaches used for the discovery and identification of selective dihydroorotate dehydrogenase inhibitors as antimalarial agents. This comprehensive review discusses recent advances in the selective therapeutic activity of distinct chemical classes of compounds as dihydroorotate dehydrogenase inhibitors and antimalarial drugs.

摘要

疟疾是一种严重的人类疾病,由于耐药菌株的存在,它已成为一个全球性的健康问题。据报道,能阻止疟原虫生长的药物作用于疟原虫生命周期的各个阶段。抗疟药物可以抑制负责疟原虫细胞生长和发育的关键酶。二氢乳清酸脱氢酶就是这样一种对嘧啶生物合成必不可少的酶。本综述重点关注用于发现和鉴定作为抗疟剂的选择性二氢乳清酸脱氢酶抑制剂的各种药物化学方法。这篇全面的综述讨论了不同化学类别的化合物作为二氢乳清酸脱氢酶抑制剂和抗疟药物在选择性治疗活性方面的最新进展。

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