首页> 外文期刊>Turkish journal of biology >Biological activities of Cu(II) and Hg(II) complexes of a heptadentate Schiff base ligand [Bir heptadentat Schiff baz ligandi{dotless}ni{dotless}n Cu(II) ve Hg(II) kompleksinin biyolojik aktivitesi]
【24h】

Biological activities of Cu(II) and Hg(II) complexes of a heptadentate Schiff base ligand [Bir heptadentat Schiff baz ligandi{dotless}ni{dotless}n Cu(II) ve Hg(II) kompleksinin biyolojik aktivitesi]

机译:七齿席夫碱配体的铜(II)和汞(II)配合物的生物活性

获取原文
获取原文并翻译 | 示例
           

摘要

Two metal complexes were synthesized as [Hg(L)](ClO_4)_2 and [Cu(L)](ClO_4)_2 by the template reaction between 2,6-bis(2-aminothiophenoxymethyl)pyridine and 2,2'-bipyridine-6,6'-dicarboxaldehyde in the presence of Hg(II) and Cu(II) perchlorate salts. The structures of the compounds were elucidated by IR, 1H-NMR, MASS, and Elemental Analyses values. Cytotoxicity of the compounds were investigated by MTT [3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide] assay in normal and cancerous rat fibroblasts. Both compounds showed cytotoxicity on 2 cell lines as a dose-dependent manner. Compound [Hg(L)](ClO_4)_2 was more cytotoxic than [Cu(L)](ClO_4)_2. Apoptotic activity of compounds was evaluated by acridine orange staining and DNA fragmentation assay. Both cell lines exposed to the compounds exhibited condensed chromatin and appearance of apoptotic bodies. The percentages of all these abnormalities were found to be very high level in ras-transformed 5RP7 fibroblasts. The effect of [Hg(L)](ClO_4)_2 was again more stronger than the compound [Cu(L)](ClO_4)_2. Although the compound [Cu(L)](ClO_4)_2 induced the formation of DNA fragmentation in both cell lines, [Hg(L)](ClO_4)_2 induced the DNA fragmentation only in cancerous 5RP7 cells, indicating specific activity. In conclusion, we suggest that both complexes, especially the one with Hg(II) according to its significant differences of apoptotic morphology and DNA fragmentation, exhibit promising potentials as anticancer compounds.
机译:通过2,6-双(2-氨基噻吩氧基甲基)吡啶与2,2'-联吡啶的模板反应合成了两种金属配合物,分别为[Hg(L)](ClO_4)_2和[Cu(L)](ClO_4)_2 Hg(II)和Cu(II)高氯酸盐存在下的-6,6'-二甲醛。化合物的结构通过IR,1 H-NMR,MASS和元素分析值来阐明。通过MTT [3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四溴化硼]测定法在正常和癌变的大鼠成纤维细胞中研究了化合物的细胞毒性。两种化合物均以剂量依赖性方式在2种细胞系上显示出细胞毒性。化合物[Hg(L)](ClO_4)_2比[Cu(L)](ClO_4)_2具有更高的细胞毒性。通过a啶橙染色和DNA片段化分析评估化合物的凋亡活性。暴露于该化合物的两种细胞系均表现出染色质浓缩和凋亡小体的外观。在ras转化的5RP7成纤维细胞中发现所有这些异常的百分比非常高。 [Hg(L)](ClO_4)_2的作用再次比化合物[Cu(L)](ClO_4)_2的作用更强。尽管化合物[Cu(L)](ClO_4)_2诱导了两个细胞系中DNA片段的形成,但是[Hg(L)](ClO_4)_2仅在癌性5RP7细胞中诱导了DNA片段的表达,显示了特定的活性。总之,我们认为这两种复合物,特别是具有Hg(II)的复合物,根据其凋亡形态和DNA片段化的显着差异,都具有作为抗癌化合物的潜在潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号