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Synthesis and Evaluation of Multifunctional Radical Quenchers for the Protection of Mitochondrial Function.

机译:用于保护线粒体功能的多功能自由基猝灭剂的合成与评价。

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摘要

Mitochondria produce the majority portion of ATP required in eukaryotic cells. ATP is generated through a process known as oxidative phosphorylation, through an pathway consisting five multi subunit proteins (complex I-IV and ATP synthase), embedded inside the mitochondrial membrane. Mitochondrial electron transport chain dysfunction increases reactive oxygen species in the cell and causes several serious disorders.;Described herein are the synthesis of antioxidant molecules to reduce the effects in an already dysfunctional system. Also described is the study of the mitochondrial electron transport chain to understand the mechanism of action of a library of antioxidants. Illustrated in chapter 1 is the general history of research on mitochondrial dysfunction and reported ways to ameliorate them. Chapter 2 describes the design and synthesis of a series of compounds closely resembling the redox-active quinone core of the natural product geldanamycin. Geldanamycin has been reported to confer cytoprotection to FRDA lymphocytes in a dose dependent manner under conditions of induced oxidative stress. A library of rationally designed derivatives has been synthesized as a part of our pursuit of a better neuroprotective drug. Chapter 3 describes the design and synthesis of a library of pyrimidinol analogues. Compounds of this type have demonstrated the ability to quench reactive oxygen species and sustain mitochondrial membrane potential.;Described herein are our efforts to increase their metabolic stability and total ATP production. It is crucial to understand the nature of interaction between a potential drug molecule and the mitochondrial electron transport chain to enable the design and synthesis a better therapeutic candidates. Chapter 4 describes a part of the enzymatic binding studies between a molecular library synthesized in our laboratory and the mitochondrial electron transport chain using sub mitochondrial particles (SMP).
机译:线粒体产生真核细胞所需的大部分ATP。 ATP是通过一种称为氧化磷酸化的过程生成的,该过程是通过包含五种多亚基蛋白(复杂的I-IV和ATP合酶)的途径嵌入线粒体膜内产生的。线粒体电子传输链功能障碍会增加细胞中的活性氧种类,并导致几种严重的疾病。本文描述了抗氧化剂分子的合成,以减少在功能失调的系统中的作用。还描述了线粒体电子传输链的研究,以了解抗氧化剂文库的作用机理。第1章介绍了线粒体功能障碍的一般研究历史,并报道了改善它们的方法。第2章介绍了一系列与天然产物格尔德霉素的氧化还原活性醌核心极为相似的化合物的设计和合成。据报道,格尔德霉素在诱导的氧化应激条件下以剂量依赖的方式赋予FRDA淋巴细胞细胞保护作用。作为我们追求更好的神经保护药物的一部分,已经合成了经过合理设计的衍生物库。第3章介绍了嘧啶醇类似物库的设计和合成。这类化合物已证明具有淬灭活性氧并维持线粒体膜电位的能力。本文描述了我们为提高其代谢稳定性和总ATP产量所做的努力。了解潜在药物分子与线粒体电子传输链之间相互作用的性质至关重要,以使设计和合成更好的治疗药物成为可能。第4章介绍了在我们实验室中合成的分子库与使用亚线粒体颗粒(SMP)的线粒体电子传输链之间的酶促结合研究的一部分。

著录项

  • 作者

    Dey, Sriloy.;

  • 作者单位

    Arizona State University.;

  • 授予单位 Arizona State University.;
  • 学科 Analytical chemistry.;Organic chemistry.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 197 p.
  • 总页数 197
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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