新型融合噻唑[3,2a]嘧啶类镇痛抗炎药的合成及生物学评价。

Nagy M Khalifa, Mohamed A Al-Omar, Abd El-Galil E Amr, Ayman R Baiuomy, Rehab F Abdel-Rahman
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引用次数: 0

摘要

采用一锅三组分法合成了几种新型的含不同取代基的双环噻唑嘧啶衍生物。通过元素分析和光谱数据证实了目标化合物的结构。研究了新合成化合物的部分成员的镇痛和抗炎活性,发现其抗炎活性明显高于吲哚美辛(对照药)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SYNTHESIS AND BIOLOGICAL EVALUATION OF SOME NOVEL FUSED THIAZOLO[3,2A]PYRIMIDINES AS POTENTIAL ANALGESIC AND ANTI-INFLAMMATORY AGENTS.

Some novel bicyclic thiazolopyrimidine derivatives bearing various substituents have been synthesized through one-pot three-component method. Structures of the target compounds were confirmed by elemental analysis and spectral data. Some selected members of the newly synthesized compounds were investigated for their analgesic and anti-inflammatory activities and revealed pronounced anti-inflammatory activity greater than that of indomethacin (reference drug).

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