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  • Original articleNew quinoxaline 1, 4-di-N-oxides: Anticancer and hypoxia-selective therapeutic agents

  • Add time:09/04/2019    Source:sciencedirect.com

    A new series of quinoxaline 1,4-di-N-oxides was synthesized and evaluated for antitumor and hypoxic-selective cytotoxic activities. Antitumor activity against liver carcinoma (Hepg2) and brain tumor (U251) human cell lines were evaluated, among the tested compounds, 5b and 9b exhibited potential cytotoxic effect against Hepg2 with IC50 values of 0.77 and 0.50 μg/mL respectively, whereas, all the tested compounds lack antitumor activity against U251 human cell line. Moreover, compound 4 was the most potent hypoxia selective-cytotoxin on EAC cell line; IC50 2.5 μg/mL, potency 22 μg/mL, and was approximately 5.4-times more selective cytotoxin (HCR > 40) than 3-amino-2-quinoxalinecarbonitrile1,4-dioxide (standard, HCR > 7.4). Compounds 8b and 9b were more selective than the standard.

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    Prev:Synthesis and antituberculosis activity of some new 2-quinoxalinecarbonitriles
    Next:Original articleSynthesis and structure–activity relationship of 3-phenylquinoxaline 1,4-di-N-oxide derivatives as antimalarial agents)

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