Department of Chemistry, Cotton University, Guwahati 781001, Assam, India.
Department of Chemistry, Cotton University, Guwahati 781001, Assam, India.
J Inorg Biochem. 2019 Nov;200:110803. doi: 10.1016/j.jinorgbio.2019.110803. Epub 2019 Aug 20.
Two new coordination complexes viz. [Mn(μ‑O,O'‑4‑Mebz)(bpy)(μ‑HO)(4‑Mebz)] (1) and [Zn(bpy)(pdc)(HO)]·3.5HO (2) (where bpy = 2,2'‑bipyridine, 4‑Mebz = 4‑methyl benzoate and pdc = 2,6‑pyridine dicarboxylate) were synthesized and structurally characterized by single crystal X-ray diffraction, FT-IR, electronic spectroscopy, Thermogravimetric Analysis (TGA) and Powder X-ray diffraction (PXRD) techniques. Complex 1 consists of a dinuclear Mn(II) unit bridged by a solvent water molecule while 2 is a mononuclear complex. The supramolecular assemblies found in the solid state of both complexes have been described. In 2, several π-stacking interactions modes have been further studied using Density Functional Theory (DFT) calculations. Furthermore, the activity of the complexes against a few pathogenic bacteria has been studied and confirmed. Finally, the antiproliferative activities of both complexes have been studied in T-cell lymphoma cell line by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, apoptosis assay and molecular docking simulation. Both the complexes exhibit gratifying cytotoxicity through apoptotic cell death with negligible cytotoxicity (~5-10%) in normal cells. It is worth mentioning that Mn(II) and Zn(II) complexes exhibit interaction modes with highly expressed cancer target proteins under study with higher binding affinity and the results are comparable with reference inhibitors.
合成了两个新的配位配合物,即[Mn(μ-O,O'-4-Mebz)(bpy)(μ-HO)(4-Mebz)](1)和[Zn(bpy)(pdc)(HO)]·3.5HO(2)(其中 bpy=2,2'-联吡啶,4-Mebz=4-甲基苯甲酸酯,pdc=2,6-吡啶二甲酸酯),通过单晶 X 射线衍射、FT-IR、电子光谱、热重分析(TGA)和粉末 X 射线衍射(PXRD)技术对其进行了结构表征。配合物 1 由一个双核 Mn(II)单元通过溶剂水分子桥接而成,而 2 是单核配合物。描述了两个配合物在固态中发现的超分子组装。在 2 中,使用密度泛函理论(DFT)计算进一步研究了几种π-堆积相互作用模式。此外,还研究了配合物对几种致病细菌的活性,并得到了证实。最后,通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法、凋亡测定法和分子对接模拟研究了两种配合物在 T 细胞淋巴瘤细胞系中的抗增殖活性。两种配合物均通过诱导细胞凋亡的方式表现出令人满意的细胞毒性,对正常细胞的细胞毒性(~5-10%)可忽略不计。值得一提的是,Mn(II)和 Zn(II)配合物与研究中高表达的癌症靶蛋白具有相互作用模式,具有更高的结合亲和力,并且结果与参考抑制剂相当。