Synthesise and test antibacterial activities of 1,3-benzodioxole derivatives

Ngoc Phuong Kieu Nguyen, Thanh Thao Vu, Ngoc Chau Tran
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Abstract

Novel chemical entities are urgently needed to develop new antibacterial agents in order to tackle the increasing antibiotic resistance. This study focuses on the 1,3-benzodioxole scaffold with promising biological activities in the literature. Five 1,3-benzodioxole containing derivatives were synthesised from piperonal as starting material by various chemical reactions. Their structures were elucidated by standard spectroscopic methods. The in vitro antibacterial activities were studied by agar diffusion method against 5 pathogenic strains: Escherichia coli, Pseudomonas aeruginosa, Enterococcus faecalis, methicillin-susceptible Staphylococcus aureus(MSSA), and methicillin-resistant Staphylococcus aureus (MRSA). The Schiff base derivative (2) showed the ability to inhibit 4/5 tested strains, including MRSA. The target prediction study suggested the in silico binding ability of (2) on the bacterial FabH enzyme. These results demonstrated that novel 1,3-benzodioxole derivatives containing Schiff bases could be further studied as new antibacterial structures.
1,3-苯二唑衍生物的合成及抗菌活性测试
为了解决日益严重的抗生素耐药性问题,迫切需要新的化学实体来开发新的抗菌药物。本研究的重点是文献中具有良好生物活性的1,3-苯二唑支架。以胡椒醛为原料,通过不同的化学反应合成了5个含1,3-苯二唑衍生物。用标准光谱方法对其结构进行了分析。采用琼脂扩散法对大肠埃希菌、铜绿假单胞菌、粪肠球菌、甲氧西林敏感金黄色葡萄球菌(MSSA)和耐甲氧西林金黄色葡萄球菌(MRSA) 5种病原菌进行体外抗菌活性研究。希夫碱衍生物(2)显示出对4/5个测试菌株的抑制能力,包括MRSA。靶标预测研究提示(2)对细菌FabH酶的硅结合能力。这些结果表明,含有席夫碱的1,3-苯二唑衍生物可以作为新的抗菌结构进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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