Center for BioEnergetics, Biodesign Institute, and Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85287, USA.
Bioorg Med Chem. 2013 Feb 15;21(4):969-78. doi: 10.1016/j.bmc.2012.11.051. Epub 2012 Dec 12.
Two new aza analogues of the neuroprotective agent idebenone have been synthesized and characterized. Their antioxidant activity, and ability to augment ATP levels have been evaluated in several different cell lines having suboptimal mitochondrial function. Both compounds were found to be good ROS scavengers, and to protect the cells from oxidative stress induced by glutathione depletion. The compounds were more effective than idebenone in neurodegenerative disease cells. These novel pyrimidinol derivatives were also shown to augment ATP levels in coenzyme Q(10)-deficient human lymphocytes. The more lipophilic side chains attached to the pyrimidinol redox core in these compounds resulted in less inhibition of the electron transport chain and improved antioxidant activity.
两种新的氮杂类似物的神经保护剂艾地苯醌已经合成和表征。其抗氧化活性,并增加在几个不同的细胞系的 ATP 水平有亚最优的线粒体功能进行了评价。这两种化合物都被发现是很好的活性氧清除剂,并能保护细胞免受谷胱甘肽耗竭引起的氧化应激。化合物比艾地苯醌在神经退行性疾病的细胞更有效。这些新型嘧啶醇衍生物也被证明能增加辅酶 Q(10)缺乏的人淋巴细胞中的 ATP 水平。在这些化合物中与嘧啶醇氧化还原核心连接的疏水性侧链导致电子传递链的抑制作用更小,抗氧化活性提高。