首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Design Synthesis and Bioactivity of N-Glycosyl-N′-(5-substituted phenyl-2-furoyl) Hydrazide Derivatives
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Design Synthesis and Bioactivity of N-Glycosyl-N′-(5-substituted phenyl-2-furoyl) Hydrazide Derivatives

机译:N-糖基-N-(5-取代的苯基-2-糠酰基)酰肼衍生物的设计合成和生物活性

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摘要

Condensation products of 5-substituted phenyl-2-furoyl hydrazide with different monosaccharides d-glucose, d-galactose,d-mannose, d-fucose and d-arabinose were prepared. The anomerization and cyclic-acyclic isomers were investigated by 1H NMR spectroscopy. The results showed that, except for the d-glucose derivatives, which were in the presence of β-anomeric forms, all derivatives were in an acyclic Schiff base form. Their antifungal and antitumor activities were studied. The bioassay results indicated that some title compounds showed superior effects over the commercial positive controls.
机译:制备了5-取代的苯基-2-呋喃酰肼与不同的单糖d-葡萄糖,d-半乳糖,d-甘露糖,d-岩藻糖和d-阿拉伯糖的缩合产物。用 1 1 H NMR光谱法研究了其异构化和环状无环异构体。结果表明,除了以β-端基异构体形式存在的d-葡萄糖衍生物以外,所有衍生物均为无环席夫碱形式。研究了它们的抗真菌和抗肿瘤活性。生物测定结果表明,某些标题化合物显示出优于商业阳性对照的效果。

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