核苷10:具有预期生物活性的新型嘧啶衍生物和融合嘧啶核苷的合成

L. M. Break, M. A. Mohamed, Ohoud A. A. Al-Thubaiti, Fatma E. M. Eibaih
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引用次数: 3

摘要

嘧啶,如6-氨基-2-硫基和2-甲基硫脲,以及稠合嘧啶,如噻吩嘧啶,与1-O-乙酰基-2,3,5-三-O-苯甲酰基-β-D-呋喃核糖反应,得到相应核苷的新衍生物。将得到的保护核苷用甲醇钠脱保护,得到相应的游离尿嘧啶和噻吩并嘧啶核苷。新形成的核苷对一些微生物(一些真菌和细菌物种)进行了生物活性测试。一些测试产品显示出中等活性,并报告了结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nucleosides 10: Synthesis of New Derivatives of Pyrimidine and Fused Pyrimidine Nucleosides of Expected Biological Activity
Pyrimidines, such as 6-amino-2-thio and 2-methylthiouracils and fused pyrimidines, such as thienopyrimidines reacted with 1-O-acetyl-2,3,5-tri-O- benzoyl-β-D-ribofuranose to get new derivatives of the corresponding nucleosides. The obtained protected nucleosides were deprotected by methanolic sodium methoxide to get the corresponding free uracil and thienopyrimidine nucleosides. The new nucleosides formed were tested for biological activity against some of microorganism (some fungi and bacteria species). Some of the tested products showed moderate activity and the results were reported.
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