Synthesis, Characterization of Pyrano-[2,3-c]-Pyrazoles Derivatives and Determination of Their Antioxidant Activities

Q4 Pharmacology, Toxicology and Pharmaceutics
Boutaina Addoum, B. E. Khalfi, Mohamed Idiken, Souraya Sakoui, Reda Derdak, O. Filali, A. Elmakssoudi, A. Soukri
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引用次数: 3

Abstract

Background: Antioxidants are developed to assist the immune system and overcome oxidative stress, the aggression of cellular constituents due to imbalance between reactive oxygen species and the inner antioxidant system. The main objective of this study was to search for new and potent antioxidants to protect humans against diseases associated with oxidative stress. Methods: In this study, three pyrano-[2,3-c]-pyrazole derivatives were synthesized via Multicomponent Reaction (MCR) approach and were characterized, using a melting point, High-Performance Liquid Chromatography (HPLC), and spectroscopic analyses (IR; 1H-NMR; 13C-NMR). All of the generated compounds were screened for their antioxidant properties in vivo, using ciliate “Tetrahymena” as a model organism exposed to oxidative and nitrative stress. They were then studied in vitro by using 1,1-diphenyl-2-picrylhydrazyl (DPPH) assays. Results: The results demonstrated that the three compounds (5a, b, c) are biologically active and possess potent antioxidant activities, especially the 5a and 5b derivatives. On the other hand, the in vitro bioassays revealed that the 5a derivative possessed a significant antioxidant activity much greater than ascorbic acid. Accordingly, the in silico data are consistent with the experimental data. Conclusion: These findings confirmed the potent antioxidant property of the synthesized compounds, providing us with new inspiration and challenges to design a library of pharmaceutical compounds with strong activity and low toxicity in the future.
吡喃-[2,3-c]-吡唑衍生物的合成、表征及抗氧化活性测定
背景:抗氧化剂是为了帮助免疫系统和克服氧化应激而开发的,氧化应激是由于活性氧和内部抗氧化系统之间的不平衡而引起的细胞成分的攻击。这项研究的主要目的是寻找新的强效抗氧化剂,以保护人类免受与氧化应激相关的疾病。方法:本研究采用多组分反应(MCR)方法合成了三种吡喃并[2,3-c]-吡唑衍生物,并用熔点、高效液相色谱(HPLC)和光谱分析(IR、1H-NMR和13C-NMR)对其进行了表征。使用纤毛虫“四膜虫”作为暴露于氧化和硝化应激的模型生物,在体内筛选所有产生的化合物的抗氧化特性。然后使用1,1-二苯基-2-苦基肼(DPPH)测定法对它们进行体外研究。结果:三个化合物(5a、b、c)均具有生物活性,并具有较强的抗氧化活性,特别是5a和5b衍生物。另一方面,体外生物测定显示,5a衍生物具有比抗坏血酸高得多的显著抗氧化活性。因此,计算机模拟数据与实验数据一致。结论:这些发现证实了合成化合物的强大抗氧化性能,为我们设计一个具有强活性和低毒性的药物化合物库提供了新的灵感和挑战。
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
Iranian Journal of Toxicology
Iranian Journal of Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
1.60
自引率
0.00%
发文量
24
审稿时长
9 weeks
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