Mohapatra Deepika, Patra Sushree Aradhana, Pattanayak Pratikshya Das, Sahu Gurunath, Sasamori Takahiro, Dinda Rupam
Department of Chemistry, National Institute of Technology, Rourkela 769008, Odisha, India.
University of Tsukuba, Institute of Natural Sciences B-506, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8571, Japan.
J Inorg Biochem. 2024 Apr;253:112497. doi: 10.1016/j.jinorgbio.2024.112497. Epub 2024 Jan 24.
Three new ONNO-donor tetradentate unsymmetrical salen ligands were synthesized by using o-phenyl diamine with substituted salicylaldehydes followed by a two-step reaction methodology. These three ligands by reaction with Cu(OAc).4HO produced three new monomeric Cu(II) complexes, [Cu(L)] (1-3). Elemental analysis, IR, UV-vis, NMR, and HR-ESI-MS techniques were used to analyze and characterize all the synthesized ligands and their corresponding metal complexes. Molecular structures of 1-3 were confirmed by the single-crystal-XRD analysis. Furthermore, the DNA binding ability of these complexes was checked through UV-vis, fluorescence spectroscopy, and also by circular dichroism studies. All the complexes were found to show an intercalation mode of binding with the K value in the range of 10-10 M. Finally, 1-3 was tested against two malignant (HeLa and A549) and non-cancerous (NIH-3T3) cell lines to check their in vitro antiproliferative activities. Among all, 1 is the most cytotoxic of the series having IC values of 5.7 ± 0.9 and 6.0 ± 0.3 μM against HeLa and A549 cell lines, respectively. This result is also consistent with the DNA binding order. Furthermore, the apoptotic mode of cell death of all the complexes was also evaluated by DAPI, AO/EB, and Annexin V-FITC/PI double staining assays.
通过邻苯二胺与取代水杨醛反应,采用两步反应方法合成了三种新型的ONNO供体四齿不对称萨伦配体。这三种配体与Cu(OAc)·4H₂O反应生成了三种新型单体Cu(II)配合物[Cu(L)](1 - 3)。采用元素分析、红外光谱、紫外可见光谱、核磁共振和高分辨电喷雾电离质谱技术对所有合成的配体及其相应的金属配合物进行了分析和表征。通过单晶X射线衍射分析确定了1 - 3的分子结构。此外,通过紫外可见光谱、荧光光谱以及圆二色性研究检测了这些配合物与DNA的结合能力。发现所有配合物均表现出插入结合模式,K值在10⁻¹⁰ M范围内。最后,对1 - 3针对两种恶性(HeLa和A549)和非癌(NIH - 3T3)细胞系进行了测试,以检查它们的体外抗增殖活性。其中,1是该系列中细胞毒性最大的,对HeLa和A549细胞系的IC值分别为5.7 ± 0.9和6.0 ± 0.3 μM。该结果也与DNA结合顺序一致。此外,还通过DAPI、AO/EB和Annexin V - FITC/PI双染色试验评估了所有配合物的细胞凋亡死亡模式。