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作为抗菌剂的芬戈莫德衍生物的合成及生物学评价

Synthesis and Biological Evaluation of Fingolimod Derivatives as Antibacterial Agents.

作者信息

Zore Matej, Gilbert-Girard Shella, Reigada Inés, Patel Jayendra Z, Savijoki Kirsi, Fallarero Adyary, Yli-Kauhaluoma Jari

机构信息

Drug Research Program, Division of Pharmaceutical Chemistry and Technology, Faculty of Pharmacy, University of Helsinki, Viikinkaari 5 E, FI-00014 Helsinki, Finland.

Drug Research Program, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, Viikinkaari 5 E, FI-00014 Helsinki, Finland.

出版信息

ACS Omega. 2021 Jul 9;6(28):18465-18486. doi: 10.1021/acsomega.1c02591. eCollection 2021 Jul 20.

Abstract

We recently identified fingolimod as a potent antibiofilm compound by screening FDA-approved drugs. To study if the antibacterial activity of fingolimod could be further improved and to explore in-depth structure-activity relationships, we synthesized 28 novel fingolimod derivatives and evaluated their efficacy against grown in planktonic/single cell and biofilms. The most effective derivatives were tested on preformed biofilms and against Gram-negative bacteria and , using fingolimod as the reference compound. Seven derivatives were more effective against , while five other derivatives showed improved activity against and/or , with no apparent change in cytotoxicity on human cells. The most interesting derivatives, compounds and , displayed a broader spectrum of antibacterial activity, possibly exerted by the change of the -hydrocarbon chain to a meta position for and by an additional hydroxyl group for .

摘要

我们最近通过筛选美国食品药品监督管理局(FDA)批准的药物,确定芬戈莫德为一种有效的抗生物膜化合物。为了研究芬戈莫德的抗菌活性是否可以进一步提高,并深入探索构效关系,我们合成了28种新型芬戈莫德衍生物,并评估了它们对浮游/单细胞生长以及生物膜的疗效。以芬戈莫德作为参考化合物,对最有效的衍生物进行了预先形成的生物膜测试,并针对革兰氏阴性菌和进行了测试。七种衍生物对更有效,而其他五种衍生物对和/或显示出改善的活性,对人类细胞的细胞毒性没有明显变化。最有趣的衍生物,即化合物和,表现出更广泛的抗菌活性谱,这可能是由于的-烃链在间位的变化以及的额外羟基所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa0f/8296573/09a5fec11d67/ao1c02591_0002.jpg

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