Center for BioEnergetics, Biodesign Institute and Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85287, United States.
Bioorg Med Chem. 2012 Sep 1;20(17):5188-201. doi: 10.1016/j.bmc.2012.07.005. Epub 2012 Jul 14.
Selected pyridinol analogues of the experimental neuroprotective drug idebenone have been synthesized and evaluated as antioxidants capable of preserving mitochondrial function. The compounds, having a different redox core but the same side chain as idebenone, exhibited a range of potencies, reflecting differences in their structures. The results obtained provide guidance in the design of such analogues with improved properties. Analogues were identified that have significantly improved antioxidant activity compared with idebenone in cultured lymphocytes, and which exhibit lesser inhibition of the electron transport chain.
已合成了实验性神经保护药物艾地苯醌的几种吡啶醇类似物,并将其评估为能够维持线粒体功能的抗氧化剂。这些化合物具有不同的氧化还原核心,但与艾地苯醌具有相同的侧链,表现出一系列的效力,反映了它们结构上的差异。所得结果为设计具有改善性能的此类类似物提供了指导。鉴定出的类似物在培养的淋巴细胞中的抗氧化活性明显优于艾地苯醌,并且对电子传递链的抑制作用较小。