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吲哚喹啉生物碱类抗疟药:进展、挑战与机遇。

Indoloquinoline Alkaloids as Antimalarials: Advances, Challenges, and Opportunities.

机构信息

Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA 02115, USA.

Department of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115, USA.

出版信息

ChemMedChem. 2024 Sep 16;19(18):e202400254. doi: 10.1002/cmdc.202400254. Epub 2024 Jul 4.

Abstract

Malaria infections affect almost half of the world's population, with over 200 million cases reported annually. Cryptolepis sanguinolenta, a plant native to West Africa, has long been used across various regions of Africa for malaria treatment. Chemical analysis has revealed that the plant is abundant in indoloquinolines, which have been shown to possess antimalarial properties. Cryptolepine, neocryptolepine, and isocryptolepine are well-studied indoloquinoline alkaloids known for their potent antimalarial activity. However, their structural rigidity and associated cellular toxicity are major drawbacks for preclinical development. This review focuses on the potential of indoloquinoline alkaloids (cryptolepine, neocryptolepine, and isocryptolepine) as scaffolds in drug discovery. The article delves into their antimalarial effects in vitro and in vivo, as well as their proposed mechanisms of action and structure-activity relationship studies. Several studies aim to improve these leads by reducing cytotoxicity while preserving or enhancing antimalarial activity and gaining insights into their mechanisms of action. These investigations highlight the potential of indoloquinolines as a scaffold for developing new antimalarial drugs.

摘要

疟疾感染影响了全球近一半的人口,每年报告的病例超过 2 亿例。原产于西非的Cryptolepis sanguinolenta 植物在非洲的许多地区长期被用于疟疾的治疗。化学分析表明,该植物富含吲哚喹啉,已被证明具有抗疟作用。Cryptolepine、neocryptolepine 和 isocryptolepine 是研究充分的吲哚喹啉生物碱,因其具有很强的抗疟活性而闻名。然而,其结构刚性和相关的细胞毒性是临床前开发的主要障碍。本综述重点介绍了吲哚喹啉生物碱(cryptolepine、neocryptolepine 和 isocryptolepine)作为药物发现中支架的潜力。文章深入探讨了它们在体外和体内的抗疟作用,以及它们的作用机制和构效关系研究。有几项研究旨在通过降低细胞毒性,同时保持或增强抗疟活性,并深入了解其作用机制来改进这些先导化合物。这些研究强调了吲哚喹啉作为开发新型抗疟药物的支架的潜力。

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