首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Cyclooctadiene Ru(II) complexes of thiophene-2-carboxaldehyde-derived thiosemicarbazones: synthesis, characterization and antiamoebic activity.
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Cyclooctadiene Ru(II) complexes of thiophene-2-carboxaldehyde-derived thiosemicarbazones: synthesis, characterization and antiamoebic activity.

机译:噻吩2-甲醛衍生的硫代半缩氮唑的环辛二烯Ru(II)配合物:合成,表征和抗厌氧活性。

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摘要

Thiosemicarbazones (TSC) 1-10 were synthesized by condensing substituted thiosemicarbazide with thiophene-2-carboxaldehyde. These thiosemicarbazones were further reacted with [Ru(eta4-C8H12)(CH3CN)2Cl2] to form complexes of the type [Ru(eta4-C8H12)(TSC)Cl2] 1a-10a. Thiosemicarbazones exhibited antiamoebic activity in the range IC50=1.09-5.42 microM. In vitro assessment of antiamoebic activity indicated that the thiosemicarbazones 3, IC50=1.67 microM, 4, IC50=1.11 microM and 6, IC50=1.09 microM showed substantially less IC50 value than metronidazole (IC50=1.87 microM), a commonly used drug against amoebiasis. Cyclooctadiene Ru(II) complexes of thiosemicarbazones showed significant improvement in antiamoebic activity (IC50=0.30-1.39 microM). All the complexes possess noteworthy potencies and showed less IC50 values than metronidazole against HK-9 strain of Entamoeba histolytica. Among all the complexes, the most promising antiamoebic activities was shown by the complexes 4a and 6a (IC50=0.31 microM of 4aand IC50=0.30 microM of 6a versus metronidazole).
机译:通过将取代的硫代氨基脲与噻吩-2-甲醛缩合,合成了硫代氨基甲酮(TSC)1-10。这些硫代半氨基甲酮进一步与[Ru(eta4-C8H12)(CH3CN)2Cl2]反应形成[Ru(eta4-C8H12)(TSC)Cl2] 1a-10a型配合物。硫代氨基脲在IC50 = 1.09-5.42 microM范围内显示出抗厌氧活性。体外抗厌氧活性评估表明,硫代半咔唑酮3,IC50 = 1.67 microM,4,IC50 = 1.11 microM和6,IC50 = 1.09 microM表现出比甲硝唑(IC50 = 1.87 microM)更低的IC50值,后者是一种常用的抗阿米巴病药物。 。硫半脲的环辛二烯Ru(II)配合物显示出明显的抗厌氧活性改善(IC50 = 0.30-1.39 microM)。所有复合物都具有显着的效价,并且显示出比甲硝唑对溶组织性变形杆菌的HK-9菌株低的IC50值。在所有配合物中,配合物4a和6a显示出最有前途的抗厌氧活性(相对于甲硝唑,IC 50 = 0.31 microM的4a和IC 50 = 0.30 microM的6a)。

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