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双环咪唑烷-4-酮衍生物的开发作为有效的抗菌剂。

Development of Bis-cyclic Imidazolidine-4-one Derivatives as Potent Antibacterial Agents.

机构信息

Department of Chemistry, University of South Florida, 4202 E. Fowler Ave, Tampa, Florida 33620, United States.

Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

出版信息

J Med Chem. 2020 Dec 24;63(24):15591-15602. doi: 10.1021/acs.jmedchem.0c00171. Epub 2020 Sep 24.

Abstract

Antibiotic resistance has emerged as one of the biggest public health concerns all over the world. In an effort to combat bacterial infections, a series of imidazolidine-4-one derivatives with potent and broad-spectrum antibacterial activity and low rates of drug resistance were developed by mimicking the salient physiochemical features of host defense peptides. These small molecules displayed potent activity against both Gram-negative and Gram-positive bacteria including several multidrug-resistant bacteria strains. Meanwhile, time-kill kinetics and drug resistance studies suggested that the most potent compound could not only eliminate the bacteria rapidly but also exhibit a low probability of drug resistance in MRSA over many passages. Further mechanistic studies suggested that eradicated bacterial pathogens by disintegrating membranes of both Gram-negative and Gram-positive bacteria. Together with their small molecular weight and low production cost compared with HDPs, these imidazolidine-4-one compounds may be developed into a new generation of antibiotic therapeutics combating emergent drug resistance.

摘要

抗生素耐药性已经成为全世界最大的公共卫生关注点之一。为了对抗细菌感染,人们通过模拟宿主防御肽的显著物理化学特征,开发了一系列具有强大广谱抗菌活性和低耐药率的咪唑烷-4-酮衍生物。这些小分子对革兰氏阴性菌和革兰氏阳性菌均具有强大的活性,包括几种多药耐药菌株。同时,时间杀伤动力学和耐药性研究表明,最有效的化合物不仅可以快速消除细菌,而且在多次传代后对 MRSA 产生耐药性的可能性也较低。进一步的机制研究表明,化合物 可以通过破坏革兰氏阴性菌和革兰氏阳性菌的细胞膜来消灭细菌病原体。与 HDP 相比,这些咪唑烷-4-酮化合物具有分子量小、生产成本低的特点,因此可能被开发成为新一代的抗生素治疗药物,用于对抗新兴的耐药性。

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