Tumor-suppressing drugs, resveratrol and quercetin, are not efficient enough to be used as chemotherapeutics.  Synthesis of novel quercetin derivatives have been prepared via ring closing of synthesized derivatives of resveratrol.  The products were characterized by <sup>1</sup>H, <sup>13</sup>C NMR spectroscopy.  The synthesized derivatives were then tested for anti-cancerous activity on cell cultures of cancerous mouse cells—one metastatic cell line (T3HA) and one non-metastatic cell line (T2A).  The results are reported for both the methoxy and amine quercetin derivatives.

Synthesis of novel quercetin derivatives for targeting of mouse cancer cell lines T3HA and T2A

251st National Meeting (2016)

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