Antimicrobial activity of some pyrazolidin-3-one Schiff base derivatives and their complexes with selected metal ions

A. A. Maihub, Sofiane Mohamed, Ahmed A Awin, Amal K Belaid, Salah M. Bensaber, Anton, Hermann, A. Gbaj
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引用次数: 3

Abstract

In spite of the fact that the structural similarity of pyrazolidin-3-one based compounds with the triazole, the antimicrobial activity of pyrazolidin-3-one compounds, have been investigated by many research groups to achieve potent antimicrobial agents. As result of the emerged drug resistance for many antimicrobial agents, we aimed in the current study to develop new potent and safe antimicrobial agents. In this study, a series of novel antimicrobial pyrazolidin-3-one based compounds and their transition metal complexes with Fe (II), Mn (II), Co(II), Ni(II), Zn(II), Cd(II), Cu(II), Pt(II) and Mo(II) ions were synthesized in good yields using microwave irradiation. All synthesized compound (free ligands and their metal complexes) were fully characterized by several spectroscopic techniques such as molar conductance, infrared, UV/Visible electronic, 1H NMR and 13C NMR spectra. In addition, the elemental analyses and conductivity investigations were done and combined with other spectroscopic data to determine the ligand: metal [M: L or L:M] ratio. The free unattached ligands and their complexes were screened for their in vitro antimicrobial activity against Staphylococcus aureus (ATCC29213) Escherichia coli (ATCC-25922), and Candida albicans (ATCC-10231). The achieved results indicated that some complexes are more potent than their free ligands and metal ions (Fe (II), Pt (II), Co(II), and Ni(II)), and some of the complexes are more potent than the standard antifungal amphoteracine-B. In conclusion, the biological activity results indicated the enhancement of the antimicrobial activity of some imine derivatives of pyrazolidin-3-one will open the field for scientists to develop more effective and safe drugs.
一些吡唑烷-3- 1希夫碱衍生物及其与选定金属离子配合物的抗菌活性
尽管吡唑烷-3-酮类化合物与三唑类化合物结构相似,但许多研究小组已经对吡唑烷-3-酮类化合物的抗菌活性进行了研究,以获得有效的抗菌药物。由于许多抗菌药物出现耐药性,我们目前的研究目标是开发新的有效和安全的抗菌药物。本研究利用微波辐照合成了一系列新型抗菌吡唑烷-3- 1基化合物及其与Fe (II)、Mn (II)、Co(II)、Ni(II)、Zn(II)、Cd(II)、Cu(II)、Pt(II)和Mo(II)离子的过渡金属配合物,收率较高。所有合成的化合物(自由配体及其金属配合物)均通过摩尔电导、红外、紫外/可见电子、1H NMR和13C NMR等多种光谱技术进行了表征。此外,进行了元素分析和电导率研究,并结合其他光谱数据确定了配体:金属[M: L或L:M]比。筛选了游离配体及其配合物对金黄色葡萄球菌(ATCC29213)、大肠杆菌(ATCC-25922)和白色念珠菌(ATCC-10231)的体外抗菌活性。结果表明,一些配合物比它们的自由配体和金属离子(Fe (II)、Pt (II)、Co(II)和Ni(II))更有效,一些配合物比标准的抗真菌药两性拉辛- b更有效。综上所述,生物活性结果表明,吡唑烷-3- 1亚胺衍生物抗菌活性的增强将为科学家开发更有效、更安全的药物开辟领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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