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Synthesis, characterization, and anticancer properties of ferrocenyl complexes containing a salicylaldehyde moiety

机译:含有水杨醛部分的二茂铁基配合物的合成,表征和抗癌性能

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A ferrocenyl ligand was prepared from condensation of 1,1'-diacetylferrocene dihydrazone with salicylaldehyde. This ligand forms 1:1 complexes with Co(II), Ni(II), Cu(II), and Zn(II) in good yield. Characterization of the ligand and complexes was carried out using infrared (IR),~1H nuclear magnetic resonance (NMR), electronic absorption, and elemental analysis. Anticancer activity of the prepared ligand and its complexes against human breast cancer cell line MCF-7 was determined, and the results were compared with the activity of the commonly used anticancer drug cisplatin. Treatments of MCF-7 cells with gradually increasing doses (5, 10, 20, and 40 μg/cm~3) of the prepared complexes revealed that the activity of superoxide dismutase and the level of hydrogen peroxide were significantly increased, while the activities of catalase and glutathione peroxidase and the levels of reduced glutathione were significantly lowered compared with in MCF-7 cells harvested from control. The results suggested that the prepared compounds possess significant anticancer activity comparable to the activity of cisplatin and may be potent anticancer agents for inclusion in modern clinical trials.
机译:由1,1′-二乙酰基二茂铁二hydr与水杨醛的缩合制备二茂铁基配体。该配体与Co(II),Ni(II),Cu(II)和Zn(II)形成1:1的配合物,收率很高。使用红外(IR),〜1H核磁共振(NMR),电子吸收和元素分析对配体和配合物进行表征。测定了所制备的配体及其复合物对人乳腺癌细胞系MCF-7的抗癌活性,并将其结果与常用的抗癌药顺铂的活性进行了比较。逐渐增加剂量(5、10、20和40μg/ cm〜3)的复合物对MCF-7细胞的处理表明,超氧化物歧化酶的活性和过氧化氢的水平显着增加,而与从对照收获的MCF-7细胞相比,过氧化氢酶和谷胱甘肽过氧化物酶以及还原型谷胱甘肽的水平显着降低。结果表明,所制备的化合物具有与顺铂活性相当的显着抗癌活性,并且可能是包含在现代临床试验中的有效抗癌剂。

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