1-(β-D-阿拉伯呋喃糖基)-5-溴-N4-取代胞嘧啶和1-(βD-阿拉伯呋喃糖基-5-溴-4-甲氧基嘧啶-2(1H)-酮衍生物的合成、细胞毒性和抗病毒活性。

R Saladino, M Mezzetti, E Mincione, A T Palamara, P Savini, S Marini
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引用次数: 3

摘要

报道了用3,3-二甲基二氧环烷选择性氧官化相应的4-硫核苷,合成了5-溴- n4 -取代-1-(β -d -阿拉伯糖醛基)胞嘧啶和5-溴- o4 -甲基-1-(β -d -阿拉伯糖醛基)嘧啶-2(1H)- 1衍生物。本文还报道了所有新合成产物的细胞毒性和对副流感1型(仙台病毒)的抗病毒活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, cytotoxic effect and antiviral activity of 1-(beta-D-arabinofuranosyl)-5-bromo-N4-substituted cytosine and 1-(beta-D-arabinofuranosyl)-5-bromo-4-methoxypyrimidin-2(1H)-one derivatives.

A convenient and mild synthesis of 5-bromo-N4-substituted-1-(beta-D-arabinofuranosyl)cytosine and 5-bromo-O4-methyl-1-(beta-D-arabinofuranosyl)pyrimidin-2(1H)-one derivatives by selective oxyfunctionalization of the corresponding 4-thionucleosides with 3,3-dimethyldioxirane is reported. The cytotoxicity and the antiviral activity against parainfluenza 1 (Sendai virus) of all new synthesized products are also reported.

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