Institute of Bioorganic & Medicinal Chemistry, Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, P. R. China.
J Med Chem. 2021 Jun 10;64(11):7630-7645. doi: 10.1021/acs.jmedchem.1c00334. Epub 2021 May 19.
A class of quinazolone thiazoles was identified as new structural scaffolds for potential antibacterial conquerors to tackle dreadful resistance. Some prepared compounds exhibited favorable bacteriostatic efficiencies on tested bacteria, and the most representative featuring the 4-trifluoromethylphenyl group possessed superior performances against and to norfloxacin. Further studies revealed that with inappreciable hemolysis could hinder the formation of bacterial biofilms and trigger reactive oxygen species generation, which could take responsibility for emerging low resistance. Subsequent paralleled exploration discovered that not only disintegrated outer and inner membranes to induce leakage of cytoplasmic contents but also broke the metabolism by suppressing dehydrogenase. Meanwhile, derivative could intercalate into DNA to exert powerful antibacterial properties. Moreover, compound gave synergistic effects against some Gram-negative bacteria in combination with norfloxacin. These findings indicated that this novel structural type of quinazolone thiazoles showed therapeutic foreground in struggling with Gram-negative bacterial infections.
一类喹唑啉噻唑类化合物被鉴定为具有潜力的抗菌征服物的新型结构支架,以应对可怕的耐药性。一些制备的化合物对测试的细菌表现出良好的抑菌效率,其中最具代表性的 4-三氟甲基苯基化合物对 和 具有优于诺氟沙星的性能。进一步的研究表明,具有可忽略不计的溶血作用的化合物 可以阻止细菌生物膜的形成并引发活性氧的产生,这可能是导致低耐药性出现的原因。随后平行探索发现,化合物 不仅破坏了内外膜,导致细胞质内容物泄漏,而且通过抑制脱氢酶来破坏代谢。同时,衍生物 可以通过嵌入 DNA 来发挥强大的抗菌作用。此外,化合物 与诺氟沙星联合使用时对一些革兰氏阴性菌具有协同作用。这些发现表明,这种新型结构类型的喹唑啉噻唑类化合物在对抗革兰氏阴性菌感染方面具有治疗前景。