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Synthesis of Pyrazolin-5-one Derivatives Clubbed with Thiazole and/or Thiadiazole and Evaluation of Their Antioxidant and Cytotoxic Activities

机译:与噻唑和/或噻二唑合成的吡唑蛋白-5-衍生物的合成以及其抗氧化剂和细胞毒性活性的评估

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摘要

Synthesis of some new thiazolyl 2-pyrazolin-5-one analogues was succeeded through the reaction of 3-methyl-1-thiocarba- moyl-2-pyrazolin-5-one with different α-halogenated deriva- tives via different routes. The physical and spectral analysis techniques were performed to demonstrate the proper structures of all incorporated analogues. The synthesized derivatives were investigated as cytotoxic agents against some important cell lines, in which the results displayed persuasive activities relative to the results of antibiotic standards. In addition, the antioxidant activity of the synthesized analogues was evaluated using ABTS;; + method. The preps analogues displayed respectable results as antioxidant agents, especially derivatives 14a-c and 11a-c due to the existence of thiadiazolyl and bis-thaizolyl arms for pyrazoline ring, respectively.
机译:通过不同的α-甲基-Moyl-2-吡唑蛋白5-酮与不同的α-卤代衍生物的反应,通过不同途径的3-甲基-1-硫代核酸-2-吡唑蛋白5-酮的反应,将一些新的噻唑基2-吡唑蛋白-5-一种类似物的合成取得了成功。 进行了物理和光谱分析技术,以证明所有合并类似物的适当结构。 研究合成的衍生物作为细胞毒性剂针对某些重要的细胞系,其中结果表现出相对于抗生素标准品的结果表现出有说服力的活性。 另外,使用ABT评估了合成类似物的抗氧化活性; +方法。 由于存在甲二二唑基和甲基二唑基臂用于吡唑啉环,因此类似物作为抗氧化剂,尤其是衍生物14A-C和11A-C显示出可观的结果。

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