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Nitroxide derivatives of non-steroidal anti-inflammatory drugs exert anti-inflammatory and superoxide dismutase scavenging properties in A459 cells

机译:非甾体类抗炎药的一氧化氮衍生物在A459细胞中发挥抗炎和超氧化物歧化酶清除作用

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摘要

BACKGROUND AND PURPOSEInflammation and reactive oxygen species are associated with the promotion of various cancers. The use of non-steroidal anti-inflammatory drugs (NSAIDs) in cancer prevention treatments has been promising in numerous cancers. We report the evaluation of NSAIDs chemically modified by the addition of a redox-active nitroxide group. TEMPO-aspirin (TEMPO-ASA) and TEMPO-indomethacin (TEMPO-IND) were synthesized and evaluated in the lung cancer cell line A549.
机译:背景和目的炎症和活性氧与多种癌症的发生有关。在许多癌症中,非甾体抗炎药(NSAID)在癌症预防治疗中的应用前景广阔。我们报告了通过添加氧化还原活性硝基基团化学修饰的非甾体抗炎药的评价。合成了TEMPO-阿司匹林(TEMPO-ASA)和TEMPO-吲哚美辛(TEMPO-IND),并在肺癌细胞系A549中进行了评估。

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