首页> 外文期刊>New Journal of Chemistry >Synthesis, structural characterization, electrochemical behavior and anticancer activity of gold(III) complexes of meso-1,2-di(1-naphthyl)-1,2-diaminoethane and tetraphenylporphyrin
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Synthesis, structural characterization, electrochemical behavior and anticancer activity of gold(III) complexes of meso-1,2-di(1-naphthyl)-1,2-diaminoethane and tetraphenylporphyrin

机译:Meso-1,2-二(1-萘基)-1,2-二氨基乙烷与四苯基卟啉金(III)配合物的合成,结构表征,电化学行为和抗癌活性

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摘要

Three gold(III) complexes, [Au(npen)Cl-2]Cl center dot 2H(2)O (1), [Au(npen)(2)]Cl-3 (2) and [Au(TPP)]Cl (3) (npen = meso-1,2-di(1-naphthyl)-1,2-diaminoethane, TPP = meso-tetraphenylporphyrin) have been synthesized and characterized using elemental analysis, IR and NMR spectroscopy, and one of them (1) by X-ray crystallography. The structure of 1 consists of a [Au(npen)Cl-2] complex ion, a chloride counter ion and two water molecules. The gold atom in the complex ion adopts a distorted square planar geometry. The interactions of 1 and 2 with L-tyrosine, glutathione and lysozyme were studied electrochemically. The electrochemical measurements indicated that gold(III) remained stable and did not undergo reduction upon interaction with proteins. The in vitro cytotoxic properties of the complexes as well as of cisplatin were evaluated on three human cancer cell lines, A549 (lung cancer cells), MCF7 (breast cancer cells) and HCT15 (colon cancer cells) using MTT assay. The results indicated that the prepared gold(III) complexes were more potent than cisplatin in inhibiting the growth of the selected cancer cells. The IC50 data revealed that complex 3 was the most effective antiproliferative agent.
机译:三种金(III)络合物,[Au(npen)Cl-2] Cl中心点2H(2)O(1),[Au(npen)(2)] Cl-3(2)和[Au(TPP)] Cl(3)(npen = meso-1,2-二(1-萘基)-1,2-diaminoethane,TPP = meso-四苯基卟啉)的合成和表征使用元素分析,IR和NMR光谱法进行,其中之一(1)通过X射线晶体学。 1的结构由[Au(npen)Cl-2]配离子,氯反离子和两个水分子组成。络合离子中的金原子采用扭曲的正方形平面几何形状。电化学研究了1和2与L-酪氨酸,谷胱甘肽和溶菌酶的相互作用。电化学测量表明,金(III)保持稳定并且在与蛋白质相互作用时未发生还原。使用MTT分析法在三种人类癌细胞系A549(肺癌细胞),MCF7(乳腺癌细胞)和HCT15(结肠癌细胞)上评估了复合物以及顺铂的体外细胞毒性。结果表明,所制备的金(III)配合物在抑制所选癌细胞生长方面比顺铂更有效。 IC50数据表明,复合物3是最有效的抗增殖剂。

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