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Antioxidant and Antitumor Activities of New Synthesized Aromatic C-Nucleoside Derivatives

机译:新合成的芳族C-核苷衍生物的抗氧化和抗肿瘤活性

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摘要

The carbohydrazide 1 was used as the precursor for the synthesis of a number of new aromatic C-nucleosides containing 1,3,4-oxadiazole 7, [1,3,4]oxadiazolo[2,3-a]isoindole 10b and pyrazole units 18. On the other hand, the thiosemicarbazone 20 was used as the key intermediate for synthesis of 1,3,4-oxadiazole and 1,2,4-triazole-3-thione derivatives 21 and 23. The antioxidant activities of the prepared compounds were evaluated. The carbohydrazide 1 in particular was found to have potent antioxidant and antitumor activity.
机译:碳酰肼1被用作前体,用于合成许多新的含有1,3,4-恶二唑7,[1,3,4]恶二唑并[2,3-a]异吲哚10b和吡唑单元的芳族C-核苷18.另一方面,将硫代半脲20用作合成1,3,4-恶二唑和1,2,4-三唑-3-硫酮衍生物21和23的关键中间体。制备的化合物的抗氧化活性被评估。特别发现了碳酰肼1具有有效的抗氧化剂和抗肿瘤活性。

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