Evaluation, Characterization of Antioxidant Activity for Novel Benzothiazole Derivatives.

Q4 Medicine
Siddhi M Chandak, Manoj R Kumbhare
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引用次数: 0

Abstract

The present study focuses on the design, synthesis, in-silico studies, characterization, and evaluation of the antidiabetic activity of nitrogen and sulphur-containing heterocyclic compounds, specifically benzothiazole derivatives (2a-2e). The synthesized compounds were characterized using spectroscopic techniques such as IR, NMR, and mass spectrometry. Their biological activity was assessed through molecular docking studies, which revealed strong binding interactions with target proteins, with compound 2a exhibiting the highest docking score (-8.7). Swiss ADME analysis was performed to evaluate pharmacokinetic properties, indicating good drug-likeness and bioavailability. In vitro antidiabetic activity was assessed using the α-amylase inhibition method, where compounds 2a and 2e demonstrated significant inhibitory potential with IC₅₀ values of 22.95±2.50µg/mL and 27.80±3.00µg/mL, respectively. These findings suggest that benzothiazole derivatives, particularly compound 2a, hold promise as potential antioxidant agents, warranting further investigation for therapeutic applications.

新型苯并噻唑衍生物抗氧化活性的评价与表征。
本研究的重点是设计、合成、硅研究、表征和评价含氮和含硫杂环化合物的抗糖尿病活性,特别是苯并噻唑衍生物(2a-2e)。合成的化合物用红外光谱、核磁共振和质谱等光谱技术进行了表征。通过分子对接研究评估了它们的生物活性,发现它们与靶蛋白有很强的结合相互作用,其中化合物2a的对接评分最高(-8.7)。瑞士ADME分析评估药代动力学性质,表明良好的药物相似性和生物利用度。采用α-淀粉酶抑制法评估体外抗糖尿病活性,其中化合物2a和2e表现出显著的抑制潜力,IC₅₀值分别为22.95±2.50µg/mL和27.80±3.00µg/mL。这些发现表明,苯并噻唑衍生物,特别是化合物2a,有望成为潜在的抗氧化剂,值得进一步研究其治疗应用。
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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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
53
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