Synthesis of water soluble copper(II) complexes: crystal structures, DNA binding, oxidative DNA cleavage, and in vitro anticancer studies

被引:0
|
作者
Tan Yi Han
Teoh Siang Guan
Muhammad Adnan Iqbal
Rosenani A. Haque
K. Sharmila Rajeswari
Mohamed B. Khadeer Ahamed
A. M. S. Abdul Majid
机构
[1] Universiti Sains Malaysia,The School of Chemical Sciences
[2] Universiti Sains Malaysia,EMAN Research and Testing Laboratory, The School of Pharmaceutical Sciences
来源
Medicinal Chemistry Research | 2014年 / 23卷
关键词
Copper(II) complexes; DNA binding; DNA cleavage; Anticancer;
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学科分类号
摘要
Two ternary copper(II) complexes of dl-threonine and polypyridyl ligands with formula of [Cu(Thr)(Byp)Cl]·H2O (1) and [Cu(Thr)(Phen)H2O]Cl·2H2O (2) were synthesized. The complexes were characterized by spectral (NMR, FT-IR, and UV–Vis), CHN elemental analysis and have been structurally elucidated by X-ray crystallography. Both of the complexes formed slightly distorted square-pyramidal coordination geometry. The electronic absorption spectra of the complexes showed a very low intensity d–d electronic band in the range of 610–620 nm in Tris–HCl/NaCl (5:5 mM) pH 7.2 buffer solution. The DNA binding interaction with calf-thymus DNA (CT-DNA) was investigated by electronic absorption spectral titration and viscosity measurements. The results revealed that the phenanthroline complex (2) interact with CT-DNA through intercalation while bipyridyl complex (1) through the groove binding mode. The calculated intrinsic binding constant (Kb) of (1) and (2) were 0.5 and 4.4 × 105 M−1, respectively. Both the complexes were found to promote efficient DNA cleavage activities at low concentration in the presence of H2O2. The results showed that (2) has the highest DNA binding and nuclease activity. Furthermore, both the complexes were tested against human colon cancer (HCT 116) and breast cancer (MCF-7) cell lines and showed a dose-dependent antiproliferation effect.
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页码:2347 / 2359
页数:12
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