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具有潜在体外抗疟原虫和体内抗耐药性恶性疟原虫活性的杂交分子。

Hybrid molecules with potential in vitro antiplasmodial and in vivo antimalarial activity against drug-resistant Plasmodium falciparum.

机构信息

WuXi AppTec Co, Ltd, Wuhan, China.

Guizhou University of Traditional Chinese Medicine, Guiyang, China.

出版信息

Med Res Rev. 2020 May;40(3):931-971. doi: 10.1002/med.21643. Epub 2019 Nov 6.

Abstract

Malaria is a tropical disease, leading to around half a million deaths annually. Antimalarials such as quinolines are crucial to fight against malaria, but malaria control is extremely challenged by the limited pipeline of effective pharmaceuticals against drug-resistant strains of Plasmodium falciparum which are resistant toward almost all currently accessible antimalarials. To tackle the growing resistance, new antimalarial drugs are needed urgently. Hybrid molecules which contain two or more pharmacophores have the potential to overcome the drug resistance, and hybridization of quinoline privileged antimalarial building block with other antimalarial pharmacophores may provide novel molecules with enhanced in vitro and in vivo activity against drug-resistant (including multidrug-resistant) P falciparum. In recent years, numerous of quinoline hybrids were developed, and their activities against a panel of drug-resistant P falciparum strains were screened. Some of quinoline hybrids were found to possess promising in vitro and in vivo potency. This review emphasized quinoline hybrid molecules with potential in vitro antiplasmodial and in vivo antimalarial activity against drug-resistant P falciparum, covering articles published between 2010 and 2019.

摘要

疟疾是一种热带疾病,每年导致约 50 万人死亡。奎宁类等抗疟药物对于对抗疟疾至关重要,但疟疾的控制受到有效药物研发管道的限制,针对抗药性疟原虫(恶性疟原虫)的药物效果有限,而这些疟原虫对目前几乎所有可用的抗疟药物都具有抗药性。为了应对日益严重的抗药性问题,急需新的抗疟药物。包含两个或多个药效团的杂交分子有可能克服抗药性,将奎宁类抗疟药效团与其他抗疟药效团杂交,可能提供具有增强的体外和体内活性的新型药物,对抗耐药性(包括多药耐药性)疟原虫。近年来,已经开发出许多奎宁类杂交药物,并对其针对一系列耐药性疟原虫株的活性进行了筛选。一些奎宁类杂交药物被发现具有有前途的体外抗疟原虫活性和体内抗疟活性,针对耐药性恶性疟原虫。本文重点介绍了具有潜在体外抗疟原虫和体内抗疟活性的奎宁类杂交分子,涵盖了 2010 年至 2019 年发表的文章。

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