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New phthalimide-appended Schiff bases: Studies of DNA binding, molecular docking and antioxidant activities

机译:新的邻近邻近邻近的席夫基地:DNA结合,分子对接和抗氧化活性的研究

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Herein, we investigated new phthalimide-based Schiff base molecules as promising DNA-binding and free radical scavenging agents. Physicochemical properties of these molecules were demonstrated on the basis of elemental analysis, ultraviolet-visible (UV-Vis), infra-red (IR), H-1 and C-13 nuclear magnetic resonance (NMR) spectroscopy. All spectral data are agreed well with the proposed Schiff base framework. The DNA-binding potential of synthesized compounds were investigated by means of UV-visible, fluorescence, iodide quenching, circular dichroism, viscosity and thermal denaturation studies. The intrinsic binding constants (K-b) were calculated from absorption studies were found to be 1.1x10(4) and 1.0x10(4)M(-1) for compounds 2a and 2b suggesting that compound 2a binding abilities with DNA were stronger than the compound 2b. Our studies showed that the presented compounds interact with DNA through groove binding. Molecular docking studies were carried out to predict the binding between Ct-DNA and test compounds. Interestingly, in silico predictions were corroborated with in vitro DNA-binding conclusions. Furthermore, the title compounds displayed remarkable antioxidant activity compared with reference standard.
机译:在此,我们研究了新的磷脂酰亚胺基氏磷酸盐基分子作为有前途的DNA结合和自由基清除剂。基于元素分析,紫外线可见(UV-VI),红外(IR),H-1和C-13核磁共振(NMR)光谱,证明了这些分子的物理化学性质。所有光谱数据都与所提出的Schiff Base框架相同。通过UV可见,荧光,碘化物猝灭,圆形二色性,粘度和热变性研究,研究了合成化合物的DNA结合潜力。对于化合物2a和2b,发现本征结合常数(Kb)从吸收研究计算为1.1×10(4)和1.0×10(4)m(-1),表明化合物2a与DNA的结合能力强于化合物2B。我们的研究表明,所提出的化合物通过沟槽结合与DNA相互作用。进行分子对接研究以预测CT-DNA和试验化合物之间的结合。有趣的是,在Silico预测中,在体外DNA结合结论中被证实。此外,与参考标准相比,标题化合物显示出显着的抗氧化活性。

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