Abstract
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. © 2014 by the authors; licensee MDPI, Basel, Switzerland.
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Cui, Z., Li, X., Tian, F., & Yan, X. (2014). Synthesis and bioactivity of 5-substituted-2-furoyl diacylhydazide derivatives with aliphatic chain. International Journal of Molecular Sciences, 15(5), 8941–8958. https://doi.org/10.3390/ijms15058941
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