首页> 外文期刊>Russian Journal of Coordination Chemistry >Antitumor Activity of Manganese(II) and Cobalt(III) Complexes of 2-Acetylpyridine Schiff Bases Derived from S-Methyldithiocarbazate: Synthesis, Characterization, and Crystal Structure of the Manganese(II) Complex of 2-Acetylpyridine S-Methyldithiocarbazate
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Antitumor Activity of Manganese(II) and Cobalt(III) Complexes of 2-Acetylpyridine Schiff Bases Derived from S-Methyldithiocarbazate: Synthesis, Characterization, and Crystal Structure of the Manganese(II) Complex of 2-Acetylpyridine S-Methyldithiocarbazate

机译:S-甲基二硫代咔唑的2-乙酰基吡啶席夫碱锰(II)和钴(III)配合物的抗肿瘤活性:2-乙酰基吡啶S-甲基二硫代咔唑的锰(II)配合物的合成,表征和晶体结构

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摘要

Transition metal complexes [Mn(L)2] (I) and [Co(L)2] · (ClO4) · H2O (II), where HL = 2-acetylpyridine S-methyldithiocarbazate, have been synthesized. Complex I was characterized by elemental analysis, IR spectra, and single-crystal X-ray diffraction studies. The manganese(II) atom in complex I adopts a distorted octahedral geometry with the Schiff base coordinated to it as a uninegatively charged tridentate chelating agent via the pyridine and azomethine nitrogen atoms and the thiolate sulfur atom. Biological studies carried out in vitro against K562 leukemia cancer cell line have shown that the free ligand and its metal complexes exhibited significant and different antitumor activity, since they exhibit IC_(50) values in the μM range.
机译:已经合成了过渡金属配合物[Mn(L)2](I)和[Co(L)2]·(ClO4)·H2O(II),其中HL = 2-乙酰吡啶S-甲基二硫代咔唑。通过元素分析,红外光谱和单晶X射线衍射研究对复合物I进行了表征。配合物I中的锰(II)原子采用扭曲的八面体几何结构,席夫碱通过吡啶和偶氮甲碱氮原子和硫醇盐硫原子与席夫碱配合作为单负电荷的三齿螯合剂。体外针对K562白血病癌细胞系进行的生物学研究表明,游离配体及其金属配合物表现出显着且不同的抗肿瘤活性,因为它们在μM范围内表现出IC_(50)值。

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