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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, characterization and antiamoebic activity of new indole-3-carboxaldehyde thiosemicarbazones and their Pd(II) complexes.
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Synthesis, characterization and antiamoebic activity of new indole-3-carboxaldehyde thiosemicarbazones and their Pd(II) complexes.

机译:新型吲哚-3-羧甲醛硫代半脲酮及其Pd(II)配合物的合成,表征和抗厌氧活性。

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摘要

In continuation of our research on thiosemicarbazones and their metal complexes as antiamoebic agents, a new series of indole-3-carboxaldehyde thiosemicarbazones (TSC) 1-7 were prepared by condensing indole-3-carboxaldehyde with cycloalkylaminothiocarbonyl hydrazines. Their palladium(II) complexes of the [Pd(TSC)Cl2] type, were synthesized upon coordination with [Pd(DMSO)2Cl2]. The chemical structures of all the compounds were established by elemental analyses, electronic, IR, (1)H NMR and (13)C NMR spectral data. The structure of the complexes was further established by thermogravimetric analysis and FAB MS. Spectroscopic data revealed that thiosemicarbazones act as bidentate ligands, making use of thione sulphur and azomethine nitrogen atom for coordination to the Pd(II) ion. Among all the compounds evaluated for antiamoebic activity using HM1:IMSS strain of Entamoeba histolytica, all palladium complexes were found to be more active than their respective ligands. Moreover, ligand 5 and complexes 1a-3a, 5a and 7a showed antiamoebic activity, at lower IC(50) doses when compared to the reference drug metronidazole with IC(50)=1.81 microM.
机译:在继续我们对作为抗厌氧剂的硫代半咔唑酮及其金属配合物的研究的基础上,通过将吲哚-3-羧甲醛与环烷基氨基硫羰基肼缩合,制得了一系列新的吲哚-3-羧甲醛硫代半咔唑酮(TSC)1-7。通过与[Pd(DMSO)2Cl2]配位,合成了[Pd(TSC)Cl2]型的钯(II)配合物。通过元素分析,电子,IR,(1)H NMR和(13)C NMR光谱数据确定所有化合物的化学结构。通过热重分析和FAB MS进一步确定了配合物的结构。光谱数据显示,硫代半脲酮可作为二齿配体,利用硫酮硫和甲亚胺氮原子与Pd(II)离子配位。在所有使用解组织变形杆菌的HM1:IMSS菌株评估的抗厌氧活性的化合物中,发现所有钯配合物均比其各自的配体更具活性。此外,与具有IC(50)= 1.81 microM的参考药物甲硝唑相比,配体5和配合物1a-3a,5a和7a在较低的IC(50)剂量下显示出抗厌氧活性。

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