Synthesis and Anticancer Effect of a Vindoline-Based Bis-Alkylated Resorcinol Derivative
Abstract
Alkylation of the simple polyphenol model resorcinol with 10-chloroacetamidovindoline resulted in the corresponding O,O-disubstituted derivative containing two elements of the Vinca alkaloid. The in vitro anticancer activity of the hybrid was investigated on the NCI-60 human tumor cell line panel, and the most important value was obtained on UO-31 renal cancer cells (50% growth inhibition GI50 = 0.893 µM).
Keywords:
resorcinol, vindoline, hybrid, anticancer effectPublished Online
2026-06-02
How to Cite
Halmai, M., Nagy, N., Mayer, S., Keglevich, P., Hazai, L. “Synthesis and Anticancer Effect of a Vindoline-Based Bis-Alkylated Resorcinol Derivative”, Periodica Polytechnica Chemical Engineering, 2026. https://doi.org/10.3311/PPch.43504
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