Synthesis and bioactivity of 5-substituted-2-furoyl diacylhydazide derivatives with aliphatic chain

12Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free