首页> 外文期刊>Inorganica Chimica Acta >Complexes of N-(2-thiazolyl)-1H-benzotriazole-1-carbothioamide with Pd(II), Pt(II), and Zn(II): Spectral, DFT, cytotoxicity and anti-angiogenic effect on MCF-7 cell line
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Complexes of N-(2-thiazolyl)-1H-benzotriazole-1-carbothioamide with Pd(II), Pt(II), and Zn(II): Spectral, DFT, cytotoxicity and anti-angiogenic effect on MCF-7 cell line

机译:N-(2-噻唑基)-1H-苯并三唑-1-碳硫酰胺与Pd(II),Pt(II)和Zn(II)的配合物:光谱,DFT,细胞毒性和对MCF-7细胞系的抗血管生成作用

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[ZnL2]center dot 4EtOH (1), [PdL(EtOH)(2)]center dot Cl (2) and [PtL(EtOH)Cl] (3) (HL = N-(2-thiazolyl)-1H-benzotriazole-1-carbothioamide complexes have been synthesized, and characterized by elemental analysis, IR, H-1 NMR, UV-Vis, and TGA. In complex 1, the thiazole N and C-S donor sites of two deprotonated ligand molecules are coordinated to Zn(II) forming a tetrahedral structure, while in case of 2 and 3, the benzotriazole N and C-S are participated in the coordination spheres of square planar complexes. Optimized structures, natural bond orbital analysis, molecular electrostatic potential maps, and frontier molecular orbitals have been obtained by DFT/B3LYP/LANL2DZ method. Time-dependent DFT calculations have been performed to assign the electronic spectra. The complexes in comparison to HL have been screened for their antimicrobial and cytotoxicity activities. Complex 2 (3.08 mu g/mL) is more potent than HL and the other complexes that may be attributed to its ionic nature and presence of two easily replaceable ethanol molecules. The capacity of complexes to slow down the proliferation of the MCF7 cell line has been achieved by down regulation of the vascular endothelial growth factors using RT-PCR technique. (C) 2014 Elsevier B.V. All rights reserved.
机译:[ZnL2]中心点4EtOH(1),[PdL(EtOH)(2)]中心点Cl(2)和[PtL(EtOH)Cl](3)(HL = N-(2-噻唑基)-1H-苯并三唑合成了-1-碳硫酰胺配合物,并通过元素分析,IR,H-1 NMR,UV-Vis和TGA对其进行了表征。在配合物1中,两个去质子化配体分子的噻唑N和CS供体与Zn( II)形成四面体结构,而在2和3的情况下,苯并三唑N和CS参与方形平面配合物的配位球,优化结构,自然键轨道分析,分子静电势图和前沿分子轨道通过DFT / B3LYP / LANL2DZ方法获得的DFT进行了时间依赖性DFT计算以指定电子光谱,筛选了与HL相比的复合物具有抗微生物和细胞毒性的活性,复合物2(3.08μg / mL)更大。比HL和其他可能由于其离子性质和pr两个易于替换的乙醇分子的本质。通过使用RT-PCR技术下调血管内皮生长因子,已经实现了复合物减缓MCF7细胞系增殖的能力。 (C)2014 Elsevier B.V.保留所有权利。

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