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抗菌药物中的螯合作用:从硝羟喹啉到头孢地尔及其他。

Chelation in Antibacterial Drugs: From Nitroxoline to Cefiderocol and Beyond.

作者信息

Repac Antić Davorka, Parčina Marijo, Gobin Ivana, Petković Didović Mirna

机构信息

Department of Microbiology and Parasitology, Faculty of Medicine, University of Rijeka, 51000 Rijeka, Croatia.

Department of Clinical Microbiology, Clinical Hospital Center Rijeka, 51000 Rijeka, Croatia.

出版信息

Antibiotics (Basel). 2022 Aug 15;11(8):1105. doi: 10.3390/antibiotics11081105.

Abstract

In the era of escalating antimicrobial resistance, the need for antibacterial drugs with novel or improved modes of action (MOAs) is a health concern of utmost importance. Adding or improving the chelating abilities of existing drugs or finding new, nature-inspired chelating agents seems to be one of the major ways to ensure progress. This review article provides insight into the modes of action of antibacterial agents, class by class, through the perspective of chelation. We covered a wide scope of antibacterials, from a century-old quintessential chelating agent nitroxoline, currently unearthed due to its newly discovered anticancer and antibiofilm activities, over the commonly used antibacterial classes, to new cephalosporin cefiderocol and a potential future class of tetramates. We show the impressive spectrum of roles that chelation plays in antibacterial MOAs. This, by itself, demonstrates the importance of understanding the fundamental chemistry behind such complex processes.

摘要

在抗菌药物耐药性不断升级的时代,开发具有新型或改进作用机制(MOA)的抗菌药物是极其重要的健康问题。增强或改善现有药物的螯合能力,或者寻找新型的、受自然启发的螯合剂,似乎是推动这一领域进展的主要途径之一。这篇综述文章从螯合作用的角度,按类别深入介绍了各类抗菌剂的作用机制。我们涵盖了广泛的抗菌药物,从具有百年历史的典型螯合剂硝羟喹啉(因其新发现的抗癌和抗生物膜活性而重新受到关注),到常用的抗菌药物类别,再到新型头孢菌素头孢地尔以及未来可能出现的一类四元环化合物。我们展示了螯合作用在抗菌药物作用机制中所发挥的广泛而重要的作用。这本身就证明了理解这些复杂过程背后基本化学原理的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ab2/9405089/f32d01ca81f1/antibiotics-11-01105-g001.jpg

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