Cui Zining, Li Xinghai, Tian Fang, Yan Xiaojing
Guangdong Province Key Laboratory of Microbial Signals and Disease Control, Department of Plant Pathology, College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510642, China.
Department of Pesticide Science, Plant Protection College, Shenyang Agricultural University, Shenyang 110866, China.
Int J Mol Sci. 2014 May 20;15(5):8941-58. doi: 10.3390/ijms15058941.
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.
设计并合成了一系列带有脂肪族链的5-取代-2-呋喃甲酰二酰肼衍生物。通过红外光谱(IR)、核磁共振氢谱(1H NMR)、元素分析和X射线单晶衍射对其结构进行了表征。抗肿瘤生物活性测试表明,一些目标化合物对所选癌细胞系表现出有前景的活性,尤其是对人早幼粒白血病细胞(HL-60)。它们的杀菌测试表明,大多数目标化合物显示出显著的抗真菌活性。初步的构效关系表明,脂肪族链长度和R2基团的差异对其抗肿瘤和抗真菌活性有明显影响。生物活性测试结果表明,这些目标化合物作为进一步药物研发的新型先导化合物具有很大的潜力。