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天然溴酚的合成甲基化和乙酰化衍生物的抗氧化及抗癌活性

Antioxidant and Anticancer Activities of Synthesized Methylated and Acetylated Derivatives of Natural Bromophenols.

作者信息

Dong Hui, Wang Li, Guo Meng, Stagos Dimitrios, Giakountis Antonis, Trachana Varvara, Lin Xiukun, Liu Yankai, Liu Ming

机构信息

Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.

Laboratory for Marine Drugs and Bioproducts of Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China.

出版信息

Antioxidants (Basel). 2022 Apr 15;11(4):786. doi: 10.3390/antiox11040786.

Abstract

Natural bromophenols are important secondary metabolites in marine algae. Derivatives of these bromophenol are potential candidates for the drug development due to their biological activities, such as antioxidant, anticancer, anti-diabetic and anti-inflammatory activity. In our present study, we have designed and synthesized a series of new methylated and acetylated bromophenol derivatives from easily available materials using simple operation procedures and evaluated their antioxidant and anticancer activities on the cellular level. The results showed that 2.,3-dibromo-1-(((2-bromo-4,5-dimethoxybenzyl)oxy)methyl)-4,5-dimethoxybenzene () and (oxybis(methylene))bis(4-bromo-6-methoxy-3,1-phenylene) diacetate () compounds ameliorated HO-induced oxidative damage and ROS generation in HaCaT keratinocytes. Compounds 2.,3-dibromo-1-(((2-bromo-4,5-dimethoxybenzyl)oxy)methyl)-4,5-dimethoxybenzene () and (oxybis(methylene) )bis(4-bromo-6-methoxy-3,1-phenylene) diacetate () also increased the TrxR1 and HO-1 expression while not affecting Nrf2 expression in HaCaT. In addition, compounds (oxybis(methylene)bis(2-bromo-6-methoxy-4,1-phenylene) diacetate () inhibited the viability and induced apoptosis of leukemia K562 cells while not affecting the cell cycle distribution. The present work indicated that some of these bromophenol derivatives possess significant antioxidant and anticancer potential, which merits further investigation.

摘要

天然溴酚是海藻中重要的次生代谢产物。这些溴酚的衍生物因其生物活性,如抗氧化、抗癌、抗糖尿病和抗炎活性,而成为药物开发的潜在候选物。在我们目前的研究中,我们使用简单的操作程序,从容易获得的材料中设计并合成了一系列新的甲基化和乙酰化溴酚衍生物,并在细胞水平上评估了它们的抗氧化和抗癌活性。结果表明,2,3 - 二溴 - 1 - ((((2 - 溴 - 4,5 - 二甲氧基苄基)氧基)甲基) - 4,5 - 二甲氧基苯()和(氧双(亚甲基))双(4 - 溴 - 6 - 甲氧基 - 3,1 - 亚苯基)二乙酸酯()化合物改善了过氧化氢诱导的HaCaT角质形成细胞中的氧化损伤和活性氧生成。化合物2,3 - 二溴 - 1 - ((((2 - 溴 - 4,5 - 二甲氧基苄基)氧基)甲基) - 4,5 - 二甲氧基苯()和(氧双(亚甲基))双(4 - 溴 - 6 - 甲氧基 - 3,1 - 亚苯基)二乙酸酯()还增加了硫氧还蛋白还原酶1(TrxR1)和血红素加氧酶 - 1(HO - 1)的表达,同时不影响HaCaT细胞中核因子E2相关因子2(Nrf2)的表达。此外,化合物(氧双(亚甲基)双(2 - 溴 - 6 - 甲氧基 - 4,1 - 亚苯基)二乙酸酯()抑制白血病K562细胞的活力并诱导其凋亡,同时不影响细胞周期分布。目前的工作表明,这些溴酚衍生物中的一些具有显著的抗氧化和抗癌潜力,值得进一步研究。

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