新型Co(II)、Ni(II)、Cu(II)和zn (II)配合物(E)-4-((喹啉-8-酰基)甲基)苯-1,2,3-三醇配体的合成、表征及体外抗癌研究

A. Sanjeev, N. Naresh Reddy, M. Kumara Swamy, Rohini Rondla, S. R. Reddy, P. Muralidhar Reddy
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引用次数: 0

摘要

本文报道了由8-氨基喹啉与2,3,4-三羟基苯甲醛缩合而成的新的三齿(NNO)希夫碱配体(E)-4-[(喹啉-8-苯基)甲基]苯-1,2,3-三醇。配体与Co(II)(1)、Ni(II)(2)、Cu(II)(3)、Zn(II)(4)等金属离子络合,并用FT-IR、UV-Vis、1HNMR、13C NMR、ESI-Mass、ESR、元素分析和磁化率等光谱和分析技术对其进行了表征。光谱数据显示钴(II)、镍(II)、铜(II)配合物呈多面体结构,锌(II)配合物呈四面体结构。对所有金属(II)配合物与希夫碱配体的抗癌活性进行了筛选。CT-DNA结合研究表明,金属配合物具有较高的结合倾向,kb值为1.50 × 104 M-1 = 1;3.62 × 104 M-1为2;3为2.53 × 104 M-1, 4为1.8 × 104 M-1。对A549和MCF-7的抗癌研究显示出良好的抗增殖活性,IC50值在17.62 ~ 48.82 μM之间。采用标准药物顺铂比较金属配合物的活性。由于其与DNA的高结合能力,这些复合物表现出显著的抗肿瘤活性。有趣的是,这些复合物对正常细胞系不产生任何细胞毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Characterization and in vitro Anticancer Studies of New Co(II), Ni(II), Cu(II) and Zn(II) Complexes of (E)-4-((Quinoline-8-ylimino)methyl)benzene-1,2,3-triol Ligand
Herein, a new tridentate (NNO) Schiff base ligand, (E)-4-[(quinoline-8-ylimino)methyl]benzene-1,2,3- triol derived from the condensation of 8-aminoquinoline with 2,3,4-trihydroxy benzaldehyde is reported. The ligand was complexed with certain metal ions like Co(II) (1), Ni(II) (2), Cu(II) (3), Zn(II) (4) and were characterized by various spectroscopic and analytical techniques such as FT-IR, UV-Vis, 1H NMR, 13C NMR, ESI-Mass, ESR, elemental analysis and magnetic susceptibility. Spectral data revealed octahedral geometry for cobalt(II), nickel(II), copper(II) complexes and tetrahedral geometry for zinc(II) complex. All the metal(II) complexes along with the Schiff base ligand were screened for their anticancer activities. The CT-DNA binding studies revealed high binding propensity for metal complexes with Kb values 1.50 × 104 M-1 for 1; 3.62 × 104 M-1 for 2; 2.53 × 104 M-1 for 3 and 1.8 × 104 M-1 for 4, respectively. Anticancer studies against A549 & MCF-7 demonstrated excellent antiproliferative activity with IC50 values in the range 17.62-48.82 μM. A standard drug cisplatin was employed to compare the activity of metal complexes. The complexes exhibited remarkable antitumour activity due to their high binding ability with DNA. It is interesting to observe that the complexes did not produce any cytotoxicity towards the normal cell lines.
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