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Synthesis, Characterization and Antitumor Studies of Two Copper(II) Schiff Base Complexes Derived from Glutathione and o-Vanillin

机译:谷胱甘肽和邻香兰素衍生的两种席夫碱铜(II)配合物的合成,表征和抗肿瘤研究

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摘要

Two new copper Schiff base complexes (Cu2C_(19)H_(31)N3O_(11)S (1), Cu2(C_(18)H_(23)N3O8S) (C_(12)H8N2)2) (2) [C_(18)H_(23)N3O8S = HL (Schiff base derived from glutathione and o-vanillin), C_(12)H8N2 = 1,10-phenanthroline] were synthesized and characterizated by elemental analysis, IR spectroscopy, 'H NMR and thermogravimetric analysis. The test of cell proliferation observed that complex 2 binding with 1,10-phenanthroline are more potent apoptosis inducers in MDA MB 231 cells than complex 1. Furthermore, our study suggests that complex 2 is capable of inhibiting tumor cellular proteasome activity and induce cancer cell-specific apoptotic death.
机译:两个新的铜席夫碱配合物(Cu2C_(19)H_(31)N3O_(11)S(1),Cu2(C_(18)H_(23)N3O8S)(C_(12)H8N2)2)(2)[C_合成(18)H_(23)N3O8S = HL(来自谷胱甘肽和邻香兰素的席夫碱),C_(12)H8N2 = 1,10-菲咯啉],并通过元素分析,红外光谱,1 H NMR和热重分析表征分析。细胞增殖测试表明,复合物2与1,10-菲咯啉的结合在MDA MB 231细胞中是比复合物1更有效的凋亡诱导剂。此外,我们的研究表明,复合物2能够抑制肿瘤细胞蛋白酶体活性并诱导癌细胞。特异性凋亡死亡。

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