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作为抗疟药的4(1)-喹诺酮衍生物针对疟原虫红细胞内期、红细胞外期及传播期的优化进展

Progress in the Optimization of 4(1)-Quinolone Derivatives as Antimalarials Targeting the Erythrocytic, the Exoerythrocytic and the Transmitting Stages of the Malaria Parasite.

作者信息

Brockmeyer Fabian, Manetsch Roman

机构信息

Northeastern University Department of Chemistry and Chemical Biology and Department of Pharmaceutical Sciences 360 Huntington Avenue, HT102, Boston, Massachusetts 02115, USA.

Northeastern University Department of Chemistry and Chemical Biology and Department of Pharmaceutical Sciences 360 Huntington Avenue, HT102, Boston, Massachusetts 02115, USA;, Email:

出版信息

Chimia (Aarau). 2017 Apr 26;71(4):213-219. doi: 10.2533/chimia.2017.213.

DOI:10.2533/chimia.2017.213
PMID:28446339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9257372/
Abstract

Malaria is one of the leading infectious diseases occurring mainly in tropical and subtropical areas. Although available antimalarial tools have reduced the number of fatalities, there is still an urgent need for the development of new and more efficacious treatments to cure and eradicate malaria especially due to emerging resistance to all antimalarial drugs. Research was initiated to revisit antimalarial compounds which were deemed unsuitable as a result of poor understanding of physicochemical properties and the optimization thereof. The 4(1H)-quinolones are a class of compounds with demonstrated activity against malaria parasites. Recent optimization of the long-known core led to two highly promising compounds, i.e. P4Q-391 and ELQ-300, with great selective activity against all stages of the parasite's life cycle and good physicochemical properties. In this paper, we discuss the key steps on the way to these compounds, which fuel hope to find a suitable treatment for the prevention, cure and eradication of malaria.

摘要

疟疾是主要发生在热带和亚热带地区的主要传染病之一。尽管现有的抗疟工具已减少了死亡人数,但仍迫切需要开发新的、更有效的治疗方法来治愈和根除疟疾,特别是由于对所有抗疟药物出现了耐药性。研究人员开始重新审视那些因对物理化学性质及其优化缺乏了解而被认为不合适的抗疟化合物。4(1H)-喹诺酮类是一类对疟原虫具有活性的化合物。最近对这一早已为人所知的核心结构进行的优化产生了两种极具前景的化合物,即P4Q-391和ELQ-300,它们对疟原虫生命周期的所有阶段都具有高度的选择性活性,并且具有良好的物理化学性质。在本文中,我们讨论了通往这些化合物的关键步骤,这些步骤为找到预防、治愈和根除疟疾的合适治疗方法带来了希望。

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本文引用的文献

1
ICI 56,780 Optimization: Structure-Activity Relationship Studies of 7-(2-Phenoxyethoxy)-4(1H)-quinolones with Antimalarial Activity.ICI 56,780的优化:具有抗疟活性的7-(2-苯氧基乙氧基)-4(1H)-喹诺酮类化合物的构效关系研究
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乙酰乙酸乙酯与高价二芳基碘鎓盐的无金属芳基化反应:直接合成多种3-芳基-4(1H)-喹诺酮类化合物
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9
4-(1H)-Quinolones and 1,2,3,4-Tetrahydroacridin-9(10H)-ones prevent the transmission of Plasmodium falciparum to Anopheles freeborni.4-(1H)-喹诺酮类和1,2,3,4-四氢吖啶-9(10H)-酮类可阻止恶性疟原虫传播至弗里伯恩按蚊。
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