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Synthesis, antioxidant and DNA cleavage activities of novel indole derivatives.

机译:新型吲哚衍生物的合成,抗氧化剂和DNA裂解活性。

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摘要

A new series of novel indole derivatives containing barbitone moiety (5a-i) are synthesized by simple and efficient condensation of chalcones (3a-i) with barbituric acid (4). The synthesized compounds are screened for their antioxidant (free radical scavenging, total antioxidant capacity and ferric reducing antioxidant power) and DNA cleavage activities were evaluated. Among the synthesized compounds (5a), (5d) and (5g) exhibited excellent antioxidant activity and all the tested compounds in the series have exhibited promising DNA cleavage activities. The structures of the synthesized compounds are assigned on the basis of elemental analysis, IR, (1)H NMR, (13)C NMR and mass spectral data.
机译:通过查耳酮(3a-i)与巴比妥酸(4)的简单有效缩合,合成了一系列新的含有巴比妥酮部分(5a-i)的吲哚衍生物。筛选合成的化合物的抗氧化剂(清除自由基,总抗氧化剂能力和三价铁还原抗氧化剂能力),并评估DNA裂解活性。在合成的化合物(5a),(5d)和(5g)中,抗氧化活性极好,该系列中所有受试化合物均显示出有希望的DNA裂解活性。根据元素分析,IR,(1)H NMR,(13)C NMR和质谱数据指定合成的化合物的结构。

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