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New platinum coordination compounds : their synthesis, characterization and anticancer application

机译:新的铂配位化合物:它们的合成,表征和抗癌应用

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摘要

The aim of this thesis was to investigate the properties of novel platinum compounds with possible potential as anticancer agents, and to determine how their behaviour could lead to a better understanding of the chemistry involved. The final criteria were improvement of their anticancer behaviour. Since many questions are still unanswered as to the role of sulfur in anticancer action, studies were undertaken to synthesize novel platinum(II) complexes having non-leaving groups consisting of a combination of an aromatic nitrogen and thioetherial sulfur capable of forming a five membered ring upon coordination. The structural unit was 1-methyl-2-methylthioalkyl/aryl. Numerous complexes formed by these ligands each having chloro, bromo, iodo and oxalato leaving groups were then fully characterized. The results obtained by the various synthetic methods were compared and explained in terms of the chemistry involved. The role of the sulfur donor was indicated in both the halo- and oxalato-complexes and proved to be strongly influenced by the nature of the leaving groups. Their differences are reflected in their anticancer behaviour. The study was extended to mononitroplatinum(IV) complexes, in view of the kinetically stable platinum(IV) compounds and advantages related to this. A specific mononitroplatinum(IV) complex which proved to have good anticancer and STAT 3 properties could according to the literature not be synthesized successfully in a good yield and a high degree of purity. The results of extensive studies showed that the main problem centred around the simultaneous reactions in equilibrium during the synthesis. A number of these species formed as a result of side reactions could be identified and their close separation factors indicated chromatographically. The mechanism of these reactions and the unstable intermediate species involved could be rationalized and compared to analogues in the literature. All the complexes studied were characterized by spectral and thermal methods both in solution as well as the solid state. Their anticancer behaviour towards three anticancer cell lines (Hela, MCF 7, Ht 29) were determined and acted as a guide towards possible structural modifications for their improved capability. Three crystal structures of platinum(II) complexes were determined. The extent of the ionization of the platinum(II) complexes as well the redox potentials (Pt(II) / Pt(IV)) of the platinum(IV) complexes were particularly important factors pertaining to their anticancer action.
机译:本文的目的是研究具有潜在潜力的新型铂化合物作为抗癌药的性质,并确定其行为如何导致对所涉及化学的更好理解。最终标准是其抗癌行为的改善。由于关于硫在抗癌作用中的作用仍有许多疑问,因此进行了研究以合成新型的具有非离去基团的铂(II)配合物,该非离去基团由能够形成五元环的芳族氮和硫醚硫的组合组成经协调。结构单元是1-甲基-2-甲基硫代烷基/芳基。然后充分表征了由这些分别具有氯,溴,碘和草酸酯离去基团的配体形成的许多络合物。比较了通过各种合成方法获得的结果,并根据所涉及的化学方法进行了解释。硫给体的作用在卤代和草酸酯络合物中均已表明,并被离去基团的性质强烈影响。他们的差异反映在他们的抗癌行为上。鉴于动力学稳定的铂(IV)化合物及其相关优点,该研究扩展到了单硝基铂(IV)配合物。根据文献,不能成功地以高收率和高纯度合成特定的单硝基铂(IV)复合物,该复合物具有良好的抗癌和STAT 3特性。大量研究的结果表明,主要问题集中在合成过程中同时发生的平衡反应上。可以确定由于副反应而形成的许多这类物质,并通过色谱法显示了它们的紧密分离系数。这些反应的机理和所涉及的不稳定中间体物种可以合理化,并与文献中的类似物进行比较。所有研究的配合物都通过光谱和热方法在溶液以及固态中进行了表征。确定了它们对三种抗癌细胞系(Hela,MCF 7,Ht 29)的抗癌行为,并作为可能对其结构进行修饰以提高能力的指南。确定了铂(II)配合物的三个晶体结构。铂(II)配合物的电离程度以及铂(IV)配合物的氧化还原电位(Pt(II)/ Pt(IV))是与它们的抗癌作用有关的特别重要的因素。

著录项

  • 作者

    Oosthuizen Lukas Marthinus;

  • 作者单位
  • 年度 2009
  • 总页数
  • 原文格式 PDF
  • 正文语种 English
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