Bioactive M(II) complexes of amino acid-based N3O donor mixed ligand: in vitro and in silico DNA binding studies.

Journal of Chemical Biology Pub Date : 2017-05-05 eCollection Date: 2017-07-01 DOI:10.1007/s12154-017-0170-3
T Daniel Prakash, V Violet Dhayabaran
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引用次数: 1

Abstract

Three novel mixed ligand M(II) complexes, namely [CoL1L2Cl2] (1), [CuL1L2Cl2] (2), and [ZnL1L2Cl2] (3), were synthesized using 1,4-naphthoquinone, L-histidine, and 1,10-phenanthroline as ligands. The ligand framework and the corresponding structural changes on complexation were ascertained based on the results of elemental analysis, conductivity measurements, magnetic behavior, FT-IR, UV-visible, 1H NMR, 13C NMR, ESR spectral studies, and ESI mass spectrometry. The biological action of the ligand (L) and complexes 1-3 such as DNA binding and cleaving ability were studied. Results suggest that the ligand and the complexes could interact with calf thymus-DNA (CT-DNA) via intercalation mode. Additionally, complex 2 displayed potential antioxidant activity in in vitro studies. Docking simulation was performed to position the ligand and the complexes into the active site of BDNA (IBNA) to determine the probable binding mode.

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以氨基酸为基础的n30供体混合配体的生物活性M(II)复合物:体外和硅DNA结合研究。
以1,4-萘醌、l -组氨酸和1,10-菲罗啉为配体,合成了[CoL1L2Cl2](1)、[CuL1L2Cl2](2)和[ZnL1L2Cl2](3)三种新型混合配体M(II)配合物。根据元素分析、电导率测量、磁性行为、FT-IR、uv -可见、1H NMR、13C NMR、ESR光谱研究和ESI质谱分析结果确定配体框架和相应的配体结构变化。研究了配体(L)和配合物1-3的生物学作用,如DNA结合和切割能力。结果表明,该配体及其复合物可通过嵌入模式与小牛胸腺dna (CT-DNA)相互作用。此外,络合物2在体外研究中显示出潜在的抗氧化活性。通过对接模拟将配体和配合物定位到BDNA (IBNA)的活性位点,确定可能的结合模式。
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