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首页> 外文期刊>Inorganica Chimica Acta >Synthesis and crystal structure determination of cobalt(II) mixed-ligand complex containing 1,10-phenanthroline and 5-(2-carboxybenzyloxy)isophthalic acid: Their biological evaluation viz. DNA/protein binding profile, pBR322 DNA cleavage activity
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Synthesis and crystal structure determination of cobalt(II) mixed-ligand complex containing 1,10-phenanthroline and 5-(2-carboxybenzyloxy)isophthalic acid: Their biological evaluation viz. DNA/protein binding profile, pBR322 DNA cleavage activity

机译:含1,10-菲咯啉和5-(2-羧苄氧基)间苯二甲酸的钴(II)混合配体配合物的合成及晶体结构测定:其生物学评价。 DNA /蛋白质结合图谱,pBR322 DNA裂解活性

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摘要

New metal-based cancer chemotherapeutic agent Co(II) complex of the type{[Co(Me(2)Phen)(o-cbiaH) (H2O)2]center dot H2O} (1) was synthesized from ligand 5-(2-carboxybenzyloxy)isophthalic acid (o-cbiaH(3)) and thoroughly characterized by spectroscopic and single crystal X-ray diffraction method. Complex 1 crystallizes in a slightly distorted octahedral CoN2O4 coordination environment. In vitro DNA binding studies of ligand and complex 1 with CT DNA were carried out by using biophysical techniques viz electronic absorption and fluorescence spectral studies which indicated that 1 binds to DNA more avidly as compared to ligand via electrostatic binding mode. Complex 1 shows significant DNA photo cleavage activity through the formation of hydroxyl radicals via photo-redox pathway. The affinity of 1 towards HSA was also investigated by the fluorescence spectroscopic technique and 3D scan measurements revealing that 1 quench the fluorescence intensity of HSA more strongly than o-cbiaH(3). Furthermore, magnetic drug targeting shows the accumulation of complex 1 in the target site under the influence of an externally applied magnetic force. (C) 2016 Elsevier B.V. All rights reserved.
机译:由配体5-(2)合成{{Co(Me(2)Phen)(o-cbiaH)(H2O)2]中心点H2O}(1)类型的新型金属基癌症化疗剂Co(II)配合物-羧基苄氧基)间苯二甲酸(o-cbiaH(3)),并通过光谱和单晶X射线衍射方法进行了全面表征。配合物1在稍微扭曲的八面体CoN2O4配位环境中结晶。配体和配合物1与CT DNA的体外DNA结合研究是通过使用生物物理技术进行的,即电子吸收和荧光光谱研究表明,与1种配体相比,通过静电结合方式与配体的结合更为亲和。配合物1通过光-氧化还原途径通过形成羟基自由基而显示出显着的DNA光裂解活性。还通过荧光光谱技术和3D扫描测量研究了1对HSA的亲和力,揭示了1比o-cbiaH(3)更强地淬灭HSA的荧光强度。此外,磁性药物靶向显示了复合物1在外部施加的磁力的影响下在靶部位的积累。 (C)2016 Elsevier B.V.保留所有权利。

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