首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >A Green Synthesis,Molecular Docking and Cytotoxicity of(E)-1-(4-(Difluoromethoxy)-2-Hydroxybenzylidene)Semicarbazide
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A Green Synthesis,Molecular Docking and Cytotoxicity of(E)-1-(4-(Difluoromethoxy)-2-Hydroxybenzylidene)Semicarbazide

机译:(E)-1-(4-(二氟甲氧基)-2-羟基苄基)氨基脲的绿色合成,分子对接和细胞毒性

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摘要

A green,one-pot three-components reaction of(E)-l-(4-(difluoromefhoxy)-2-hydroxybenzylidene)semicarbazide has been designed,synthesized and characterized by elemental,FT-IR,~1H and ~(l3)C NMR spectral data.The cytotoxic activities of the synthesized/compound were evaluated by MTT assay in human cancer cell lines.Docking studies of 3-substituted indolin-2-one scaffolds on vasculaf endothelial growth factor receptor 2(VEGFR-2)involved in cell proliferation and angiogenesis was performed.Based on the ligand efficiency indices,Scruff bases may be regarded as efficient candidates for further molecular developments of anticancer agents.The molecule is useful in sensing and drug-carrying applications.
机译:(e)-1-(4-(二氟聚硼氧基)-2-羟基苄基)氨基脲的一种绿色,一锅三分 - (4-(二氟聚氢氧基)-2-羟基苄基),通过元素,FT-IR,〜1H和〜(L3)合成和表征 C NMR光谱数据。通过MTT测定在人癌细胞系中的MTT测定来评价合成/化合物的细胞毒性活性。涉及的血管内皮生长因子受体2(VEGFR-2)上的3取代的Indolin-2-1支架的载体研究 进行细胞增殖和血管生成。基于配体效率指标,可瘢痕碱碱基被认为是抗癌剂的进一步分子发育的有效候选者。分子可用于感测和携带药物的应用。

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