Abstract :
Quercetin, a ubiquitous flavonol, represents a promising leading drug for development of
new chemotherapeutic agents. However, its limited cytotoxicity to cancer cells hampers its
clinical use. In order to obtain novel quercetin derivatives with superior cytotoxicity, seven
alkylated quercetin derivatives were synthesized. Solubility of these derivatives was determined
by turbidimetry. Cytotoxicity of the high-soluble derivatives against MCF-7 cells and caco-
2 cells was determined using MTT assay. Among these seven products, 7-O-butylquercetin
had the highest solubility in DMEM medium and 7-O-geranylquercetin had the most
potent cytotoxicity. Further study on cytotoxicity of 7-O-geranylquercetin on NCI-H446,
A549, MGC-803 and SGC-7901 cell lines revealed potential antiproliferative effects. The
7-O-geranylquercetin is a broad spectrum cytotoxic agent and it may be a promising leading
drug for cancer chemotherapy
Keywords :
Quercetin , Alkyl derivatives , Cytotoxicity , Selective alkylation