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Synthesis and anticancer activity of silver(I)–N-heterocyclic carbene complexes derived from the natural xanthine products caffeine, theophylline and theobromine

机译:来自天然黄嘌呤产品咖啡因,茶碱和可可碱的银(I)-N-杂环卡宾配合物的合成和抗癌活性

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摘要

A new library of silver(I)–N-heterocyclic carbene complexes prepared from the natural products caffeine, theophylline and theobromine is reported. The complexes have been fully characterised using a combi- nation of NMR spectroscopy, mass spectrometry, elemental analysis and X-ray diffraction analysis. Fur- thermore, the hydrophobicity of the complexes has been measured. The silver(I)–N-heterocyclic carbenes have been evaluated for their antiproliferative properties against a range of cancer cell lines of different histological types, and compared to cisplatin. The data shows different profiles of response when compared to cisplatin in the same panel of cells, indicating a different mechanism of action. Furthermore, it appears that the steric effect of the ligand and the hydrophobicity of the complex both play a role in the chemosensitivity of these compounds, with greater steric bulk and greater hydrophilicity delivering higher cytotoxicity
机译:据报道,由天然产物咖啡因,茶碱和可可碱制备的银(I)-N-杂环卡宾配合物的新库。使用NMR光谱,质谱,元素分析和X射线衍射分析的组合已对复合物进行了充分表征。此外,已经测量了配合物的疏水性。已经评估了银(I)-N-杂环卡宾对多种不同组织学类型的癌细胞系的抗增殖特性,并与顺铂进行了比较。与同一组细胞中的顺铂相比,数据显示了不同的反应曲线,表明了不同的作用机制。此外,似乎配体的空间效应和复合物的疏水性均在这些化合物的化学敏感性中起作用,更大的空间体积和更大的亲水性带来更高的细胞毒性。

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