Review of anticancer mechanisms of isoquercitin

doi:10.5306/wjco.v7.i2.189

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Apr 10, 2016 (publication date) through Dec 26, 2024

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World Journal of Clinical Oncology

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2218-4333

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Oncol. Apr 10, 2016; 7(2): 189-199
Published online Apr 10, 2016. doi: 10.5306/wjco.v7.i2.189

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Figure 1 Basic structure of Flavonols. Flavonols have one hydroxyl (OH) group on the third carbon (C3) and one carbonyl group (C=O) on the fourth carbon (C4) of the C ring [2]².

Citation: Orfali GDC, Duarte AC, Bonadio V, Martinez NP, de Araújo MEMB, Priviero FBM, Carvalho PO, Priolli DG. Review of anticancer mechanisms of isoquercitin. World J Clin Oncol 2016; 7(2): 189-199
URL: https://www.wjgnet.com/2218-4333/full/v7/i2/189.htm
DOI: https://dx.doi.org/10.5306/wjco.v7.i2.189