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作为抗肿瘤和抗病毒药物的4'-硫代核苷的合成。

Synthesis of 4'-Thionucleosides as Antitumor and Antiviral Agents.

作者信息

Yoshimura Yuichi, Saito Yukako, Natori Yoshihiro, Wakamatsu Hideaki

机构信息

Faculty of Pharmaceutical Sciences, Tohoku Medical and Pharmaceutical University.

出版信息

Chem Pharm Bull (Tokyo). 2018;66(2):139-146. doi: 10.1248/cpb.c17-00636.

Abstract

Many attempts have been made to synthesize structurally novel nucleoside derivatives in order to identify effective compounds for the treatment of tumors and virus-caused disease. At our laboratories, as part of our efforts to synthesize 4'-thionucleosides, we have identified and characterized biologically active nucleosides. During the course of our synthetic study, we developed the Pummerer-type thioglycosylation reaction. As a result, we synthesized a potent antineoplastic nucleoside, 1-(2-deoxy-2-fluoro-β-D-4-thio-arabino-furanosyl)cytosine (4'-thioFAC), and several novel 4'-thionucleosides that possess antiherpes virus activities.

摘要

为了鉴定出治疗肿瘤和病毒引起疾病的有效化合物,人们已进行了许多尝试来合成结构新颖的核苷衍生物。在我们实验室,作为合成4'-硫代核苷工作的一部分,我们已鉴定并表征了具有生物活性的核苷。在我们的合成研究过程中,我们开发了Pummerer型硫代糖基化反应。结果,我们合成了一种有效的抗肿瘤核苷,1-(2-脱氧-2-氟-β-D-4-硫代阿拉伯呋喃糖基)胞嘧啶(4'-硫代FAC),以及几种具有抗疱疹病毒活性的新型4'-硫代核苷。

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