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新型具有强抗氧化活性的基于大麻二酚的衍生物的设计、合成与表征。

Design, Synthesis, and Characterization of Novel Cannabidiol-Based Derivatives with Potent Antioxidant Activities.

机构信息

Department of Biotechnology, Tel-Hai Academic College, Kiryat Shmona 11016, Israel.

Natural Compounds and Organic Synthesis Laboratory, Migal-Galilee Research Institute, Kiryat Shmona 11016, Israel.

出版信息

Int J Mol Sci. 2024 Sep 4;25(17):9579. doi: 10.3390/ijms25179579.

Abstract

In recent years, extensive research has focused on cannabidiol (CBD), a well-studied non-psychoactive component of the plant-derived cannabinoids. CBD has shown significant therapeutic potential for treating various diseases and disorders, including antioxidants and anti-inflammatory effects. Due to the promising therapeutic effect of CBD in a wide variety of diseases, synthetic derivatization of this compound has attracted the attention of drug discovery in both industry and academia. In the current research, we focused on the derivatization of CBD by introducing Schiff base moieties, particularly (thio)-semicarbazide and aminoguanidine motifs, at the 3-position of the olivetolic ring. We have designed, synthesized, and characterized new derivatives based on CBD's framework, specifically aminoguanylhydrazone- and (thio)-semicarbazones-CBD-aldehyde compounds. Their antioxidant potential was assessed using FRAP and DPPH assays, alongside an evaluation of their effect on LDL oxidation induced by Cu and AAPH. Our findings suggest that incorporating the thiosemicarbazide motif into the CBD framework produces a potent antioxidant, warranting further investigation.

摘要

近年来,人们对大麻二酚(CBD)进行了广泛的研究,它是植物来源的大麻素中一种研究充分的非精神活性成分。CBD 在治疗各种疾病和病症方面具有显著的治疗潜力,包括抗氧化和抗炎作用。由于 CBD 在广泛的疾病中具有有前景的治疗效果,因此该化合物的合成衍生引起了工业界和学术界药物发现的关注。在当前的研究中,我们专注于 CBD 的衍生化,通过在橄榄环的 3 位引入席夫碱部分,特别是(硫)-半缩氨和氨基胍基 motif。我们设计、合成并表征了基于 CBD 骨架的新型衍生物,特别是氨基胍基酰肼和(硫)-半缩氨甲酰基-CBD-醛化合物。使用 FRAP 和 DPPH 测定法评估了它们的抗氧化潜力,并评估了它们对 Cu 和 AAPH 诱导的 LDL 氧化的影响。我们的研究结果表明,将硫代半缩氨甲酰基引入 CBD 骨架可产生一种有效的抗氧化剂,值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c43/11395037/16577ccc9e31/ijms-25-09579-g001.jpg

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