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Synthesis and biological activity of some pyrimidine derivatives.

机译:一些嘧啶衍生物的合成和生物活性。

摘要

To synthesize a variety of pyrimidine analogs, 3, 4, 5, 6(a–d), 7(a–d) and their anticonvulsant and antioxidant activity was determined.udMethods Using 5-bromo-2,4-dichloropyrimidine and hydrazine hydrate, new compounds were synthesized. The structures of all the new compounds are established on the basis of FT-IR, 1H NMR and mass spectral data. Anticonvulsant study was done by MES seizure model and rotorod method was employed to determine the neurotoxicity. Antioxidant activity was done by DPPH method.udResults All the compounds were synthesized in good yield. Among the new compounds, 6c and 7c are found to be most potent and showed no neurotoxicity. All the compounds showed DPPH radical scavenging activity, where compounds 7b, 7a and 6b were the best radical scavengers.
机译:为了合成各种嘧啶类似物,分别测定3、4、5、6(a-d),7(a-d)及其抗惊厥和抗氧化活性。 ud方法使用5-溴-2,4-二氯嘧啶和肼水合物,合成了新化合物。所有新化合物的结构都是基于FT-IR,1H NMR和质谱数据确定的。通过MES癫痫模型进行抗惊厥研究,并采用旋翼法测定神经毒性。结果:所有化合物均以良好的收率合成。在新化合物中,发现6c和7c最有效,并且没有神经毒性。所有化合物均显示出DPPH自由基清除活性,其中化合物7b,7a和6b是最佳的自由基清除剂。

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