| Literature DB >> 32914977 |
Minghui Wang1, Ruixuan Gao1, Mengmeng Zheng1, Peng Sang1, Chunpu Li1,2, En Zhang1,3, Qi Li2, Jianfeng Cai1.
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 3 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 3 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.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32914977 PMCID: PMC8903082 DOI: 10.1021/acs.jmedchem.0c00171
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446