Pd (II)配合物的生物学影响:合成、光谱表征、体外抗癌、CT-DNA结合和抗氧化活性

N. Sharma, R. K. Ameta, Man Singh
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引用次数: 12

摘要

合成了一系列新的甲基取代苄胺配体Pd (II)配合物,并用紫外/可见等光谱技术对其进行了表征。FTIR, LCMS, 1H和13C NMR。在DMSO、DMSO +水和DMSO + PBS缓冲液(pH = 7.2)中的UV/Vis研究证实了它们在液体中的分子可持续性。它们对乳腺癌细胞系如MCF-7和MDA-MB-231的体外抗癌活性使其对体内分析很有兴趣。与游离配体相比,它们具有较强的DNA结合活性(DBA),是一种较好的DNA结合剂。理化研究进一步证实了DBA,如复合物+ DNA的表面张力和粘度,分别推断DNA的破坏和复合物的插入。本文首次报道了它们的%结合活性、% DNA碱基对破坏率(DNABP)和%插层强度,以便更好地了解DNA的结合机制。同时,通过DPPH自由基测定其清除活性(SA),结果表明配合物具有良好的抗氧化性能。
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Biological Impact of Pd (II) Complexes: Synthesis, Spectral Characterization, In Vitro Anticancer, CT-DNA Binding, and Antioxidant Activities
A new series of Pd (II) complexes of methyl substituted benzylamine ligands (BLs) has been synthesized and characterized via spectroscopic techniques such as UV/Vis. FTIR, LCMS, 1H, and 13C NMR. The UV/Vis study in DMSO, DMSO + water, and DMSO + PBS buffer (pH = 7.2) confirmed their molecular sustainability in liquids. Their in vitro anticancer activity against breast cancer cell lines such as MCF-7 and MDA-MB-231 makes them interesting for in vivo analysis. Their stronger DNA binding activity (DBA) compared with free ligand suggested them as a good DNA binder. DBA was further confirmed by physicochemical studies such as surface tension and viscosity of complex + DNA which inferred the disruption of DNA and intercalation of complexes, respectively. Their % binding activity, % disruption of DNA base pairs (DNABP), and % intercalating strength are reported in this paper for the first time for better understanding of DNA binding mechanism. Along with this, their scavenging activity (SA) determined through DPPH free radical and the results indicate good antioxidant behaviour of complexes.
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期刊介绍: International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis. International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis.
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