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Synthesis and Bioactivity of 5-Substituted-2-furoyl Diacylhydazide Derivatives with Aliphatic Chain

机译:具有脂肪链的5-取代的-2-呋喃基二酰基酰肼衍生物的合成及生物活性

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摘要

A series of 5-substituted-2-furoyl diacylhydazide derivatives with aliphatic chain were designed and synthesized. Their structures were characterized by IR, 1H NMR, elemental analysis, and X-ray single crystal diffraction. The anti-tumor bioassay revealed that some title compounds exhibited promising activity against the selected cancer cell lines, especially against the human promyelocytic leukemic cells (HL-60). Their fungicidal tests indicated that most of the title compounds showed significant anti-fungal activity. The preliminary structure-activity relationship showed that the aliphatic chain length and differences in the R2 group had obvious effects on the anti-tumor and anti-fungal activities. The bioassay results demonstrated that the title compounds hold great promise as novel lead compounds for further drug discovery.
机译:设计并合成了一系列具有脂肪族链的5-取代-2-糠酰基二酰基酰肼衍生物。通过IR,1 H NMR,元素分析和X射线单晶衍射对它们的结构进行了表征。抗肿瘤生物测定表明,某些标题化合物对选定的癌细胞系,特别是对人类早幼粒细胞白血病细胞(HL-60)表现出有希望的活性。他们的杀菌测试表明,大多数标题化合物均显示出显着的抗真菌活性。初步的构效关系表明,脂族链长和R 2 基团的差异对抗肿瘤和抗真菌活性有明显影响。生物测定结果表明,标题化合物作为用于进一步药物发现的新型先导化合物具有广阔的前景。

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