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Synthesis and antiviral and cytostatic activities of carbocyclic nucleosides incorporating a modified cyclobutane ring. Part 1: Guanosine analogues.

机译:含有修饰的环丁烷环的碳环核苷的合成以及抗病毒和细胞抑制活性。第1部分:鸟苷类似物。

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摘要

Five new carbocyclic nucleosides were prepared by constructing a guanine (compounds 3, 5) or 8-azaguanine (compounds 4, 6, and 7) base on the amino group of (1'S,3'R)-3-(3'-amino-2',2'-dimethylcyclobutyl)propan-1-ol (8), and their activities against a variety of viruses and tumor cell lines were determined. Only compounds 3 and 7 showed a detectable activity at subtoxic concentrations against some viruses tested.
机译:通过基于(1'S,3'R)-3-(3'-氨基)的氨基构建鸟嘌呤(化合物3、5)或8-氮杂鸟嘌呤(化合物4、6和7)制备了五个新的碳环核苷确定了-2',2'-二甲基环丁基)丙-1-醇(8)及其对多种病毒和肿瘤细胞系的活性。只有化合物3和7在亚毒性浓度下对某些测试病毒显示出可检测的活性。

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