Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids

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Abstract

Hybrid compounds of flavones, namely chrysin and kaempferol, and substituted 1,2,3-triazole derivatives, were synthesized by click reaction of the intermediate O-propargyl derivatives. 4-Fluoro- and 4-nitrobenzyl-1,2,3-triazole-containing hybrid molecules were prepared. The mono- and bis-coupled hybrids were investigated on 60 cell lines of 9 common cancer types (NCI60) in vitro as antitumor agents. Some of them proved to have a significant antiproliferative effect.

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Németh-Rieder, A., Keglevich, P., Hunyadi, A., Latif, A. D., Zupkó, I., & Hazai, L. (2023). Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids. Molecules, 28(2). https://doi.org/10.3390/molecules28020626

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