Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, Yangling, China.
Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, Yangling, China.
Bioorg Med Chem Lett. 2023 Jun 1;89:129320. doi: 10.1016/j.bmcl.2023.129320. Epub 2023 May 6.
Herein, a series of novel indole-piperazine derivatives were synthesized. Bioassay results showed the title compounds exhibited moderate to good bacteriostatic efficacy against the test Gram-positive bacteria and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). Among theses compounds, three remarkable compounds 8f, 9a, and 9h exhibited superior in vitro antibacterial profiles for anti- S. aureus and anti-MRSA to that of gentamicin. Hit compound 9a manifested a rapid bactericidal kinetic effect on MRSA, with no resistance observed after 19 days of sequential passaging. And 8 µg/mL of compound 9a displayed considerable post antibacterial effects to that of ciprofloxacin at the concentration of 2 µg/mL. Cytotoxic and ADMET studies indicated, to some extent, compounds 8f, 9a, and 9h were up to the standard for antibacterial drugs. These results suggest that indole/piperazine derivatives based on the title compounds can serve as a new scaffold for antimicrobial development.
本文合成了一系列新型吲哚哌嗪衍生物。生物测定结果表明,标题化合物对测试的革兰氏阳性菌和革兰氏阴性菌具有中等至良好的抑菌效果,包括耐甲氧西林金黄色葡萄球菌(MRSA)。在这些化合物中,三个显著的化合物 8f、9a 和 9h 对金黄色葡萄球菌和抗 MRSA 的体外抗菌谱优于庆大霉素。化合物 9a 对 MRSA 表现出快速的杀菌动力学效应,在连续传代 19 天后未观察到耐药性。并且 8μg/mL 的化合物 9a 在浓度为 2μg/mL 时表现出与环丙沙星相当的后抗菌作用。细胞毒性和 ADMET 研究表明,在某种程度上,化合物 8f、9a 和 9h 符合抗菌药物的标准。这些结果表明,基于标题化合物的吲哚/哌嗪衍生物可以作为抗菌药物开发的新骨架。