| Literature DB >> 34520955 |
Yongzhi Chen1, Hongxia Li1, Jiayong Liu1, Rongcui Zhong1, Haizhou Li1, Shanfang Fang1, Shouping Liu2, Shuimu Lin3.
Abstract
The emergence of bacterial multidrug resistance and the lack of new antimicrobial agents urgently demand the discovery and development of novel antibacterials that avoid bacterial resistance. Antimicrobial peptidomimetics represent a promising approach for overcoming antibiotic resistance. Herein we report the synthesis and evaluation of indole-based amphiphilic antimicrobial peptidomimetics, bearing hydrophobic side chains and hydrophilic cationic moieties. Among these derivatives, compound 28 demonstrated potent antimicrobial activity against Gram-positive bacteria, low hemolytic activity and low toxicity towards mammalian cells, as well as good stability in salt conditions. Moreover, compound 28 showed the rapid killing of bacteria via membrane-targeting action without developing bacterial resistance. More importantly, compound 28 displayed high antimicrobial potency against Gram-positive bacteria in a murine model of bacterial keratitis, and was found to be more efficient than vancomycin. Thus, compound 28 had great potential as a promising lead compound for the treatment of Gram-positive bacterial infection.Entities:
Keywords: Antimicrobial agents; Bacterial resistance; Indole; Membrane-targeting; Peptidomimetics
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Year: 2021 PMID: 34520955 DOI: 10.1016/j.ejmech.2021.113813
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514