咪唑[4,5-d]吡啶衍生物的合成及其抗氧化和抗菌活性

IF 3.3 Q2 MULTIDISCIPLINARY SCIENCES Scientific African Pub Date : 2025-03-01 Epub Date: 2025-02-27 DOI:10.1016/j.sciaf.2025.e02625
Soukaina Benkirane , Zineb El-Jabri , Houria Misbahi , Safia Sabir , Amin Laglaoui , Khalid Misbahi
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引用次数: 0

摘要

这项工作涵盖了咪唑[4,5-d]吡啶系列的多功能能力,该系列先前设计、合成并测试了其腐蚀、抑制活性以及对酪氨酸- trna合成酶活性的抑制。该研究扩展到它们的抗菌和抗氧化能力的评价。特别是化合物1c显示出显著的抗氧化作用,突出了抗氧化应激的潜在应用。抗菌研究显示其有效性,特别是对金黄色葡萄球菌,提示有针对性的抗菌应用。此外,抗真菌评价表明,化合物1c(2-苯基硝基在2位)也能抑制尖孢镰刀菌的菌丝生长,从而拓宽了其生物活性谱。这些结果不仅强调了咪唑吡啶衍生物的多种药理潜力,而且为未来的药物设计和开发提供了重要信息。
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Synthesis, Antioxidant and antimicrobial activities of some imidazo[4,5-d]pyridine derivatives
This work covers the multifunctional capabilities of imidazo[4,5-d]pyridine series, previously designed, synthesized and tested for its corrosion, inhibitory activity, as well as its inhibition of tyrosyl-tRNA synthetase activity. The study extends to the evaluation of their antimicrobial and antioxidant capacities. In particular, compound 1c shows significant antioxidant effects, highlighting potential applications against oxidative stress. Antibacterial studies reveal its efficacy, particularly against Staphylococcus aureus, suggesting targeted antibacterial applications. Furthermore, antifungal evaluations revealed that compound 1c (with 2-phenylnitro group in position 2) can also inhibit the mycelial growth of Fusarium oxysporum, thus broadening its spectrum of bioactivity. These results not only underline the diverse pharmacological potential of imidazopyridine derivatives but also provide crucial information for future drug design and development.
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来源期刊
Scientific African
Scientific African Multidisciplinary-Multidisciplinary
CiteScore
5.60
自引率
3.40%
发文量
332
审稿时长
10 weeks
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