Pyridyl Thiosemicarbazone Complexes of Ni (II), Cu (II), and Zn (II): Structural Insights and Neuropharmacological Activity

IF 4.3 2区 化学 Q2 CHEMISTRY, APPLIED
Nishant Shekhar, Rajesh Kumar, Riya Kumari, Ram Nayan Gautam, Diptee Mitra, Ramesh Chandra, Arti Srivastava, M. K. Bharty
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Abstract

Thiosemicarbazone-based metal complexes have attracted considerable attention due to their rich coordination chemistry and emerging biological relevance; however, systematic correlations between their structural features and neuropharmacological activities remain limited. In this work, three metal complexes, [Ni(HcpmTsc)2] (1), [Cu(HcpmTsc)(Cl)] (2), and [Zn(HcpmTsc)2] (3), derived from N-(2-chlorophenyl)-2-(pyridyl methylene) thiosemicarbazone (H2cpmTsc), were synthesized and comprehensively characterized using spectral techniques. In addition, complexes 1 and 3 were characterized by single-crystal X-ray diffraction, whereas the crystal structure of complex 2 had been reported earlier; however, its sedative and anxiolytic activities have been evaluated for the first time in the present study. Structural analyses revealed distorted octahedral geometries for complexes 1 and 3, with the ligand acting as a uninegative tridentate donor in all cases. The crystal structures reveal extended supramolecular assemblies stabilized by intermolecular C-H···N and C-H···S interactions. Photoluminescence studies demonstrated that the ligand and all complexes exhibit fluorescent behavior. To address the paucity of neuropharmacological investigations on such systems, the synthesized compounds were evaluated for sedative and anxiolytic activities using established animal models. The results indicated notable sedative and anxiolytic effects mediated predominantly through GABAA receptor pathways, with [Ni(HcpmTsc)2] (1) showing the highest activity. Molecular docking studies supported these findings by confirming favorable receptor interactions. Overall, this study highlights the therapeutic potential of these complexes as candidates for neuropharmacological development.

吡啶基硫代氨基脲配合物的Ni (II), Cu (II)和Zn (II):结构见解和神经药理活性
巯基氨基脲类金属配合物因其丰富的配位化学和新兴的生物学相关性而受到广泛关注;然而,它们的结构特征与神经药理活性之间的系统相关性仍然有限。本文合成了由N-(2-氯苯基)-2-(吡啶基亚甲基)硫代氨基脲(H2cpmTsc)衍生的金属配合物[Ni(HcpmTsc)2](1)、[Cu(HcpmTsc)(Cl)](2)和[Zn(HcpmTsc)2](3),并利用光谱技术对其进行了综合表征。此外,配合物1和3通过x射线单晶衍射进行了表征,而配合物2的晶体结构早前已被报道;然而,本研究首次对其镇静和抗焦虑活性进行了评价。结构分析揭示了配合物1和3的扭曲八面体几何形状,配体在所有情况下都作为非负的三叉戟供体。晶体结构显示出由分子间C-H··N和C-H··S相互作用稳定的扩展的超分子组合。光致发光研究表明,配体和所有配合物都表现出荧光行为。为了解决这类系统神经药理学研究的缺乏,我们利用已建立的动物模型评估了合成的化合物的镇静和抗焦虑活性。结果显示,其镇静和抗焦虑作用主要通过GABAA受体途径介导,其中[Ni(HcpmTsc)2](1)的活性最高。分子对接研究通过确认有利的受体相互作用支持了这些发现。总的来说,这项研究强调了这些复合物作为神经药理学发展候选物的治疗潜力。
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来源期刊
Applied Organometallic Chemistry
Applied Organometallic Chemistry 化学-无机化学与核化学
CiteScore
7.80
自引率
10.30%
发文量
408
审稿时长
2.2 months
期刊介绍: All new compounds should be satisfactorily identified and proof of their structure given according to generally accepted standards. Structural reports, such as papers exclusively dealing with synthesis and characterization, analytical techniques, or X-ray diffraction studies of metal-organic or organometallic compounds will not be considered. The editors reserve the right to refuse without peer review any manuscript that does not comply with the aims and scope of the journal. Applied Organometallic Chemistry publishes Full Papers, Reviews, Mini Reviews and Communications of scientific research in all areas of organometallic and metal-organic chemistry involving main group metals, transition metals, lanthanides and actinides. All contributions should contain an explicit application of novel compounds, for instance in materials science, nano science, catalysis, chemical vapour deposition, metal-mediated organic synthesis, polymers, bio-organometallics, metallo-therapy, metallo-diagnostics and medicine. Reviews of books covering aspects of the fields of focus are also published.
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