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4'-C-甲基-2'-氟阿拉伯核苷的合成与抗癌活性评价

Synthesis and anticancer evaluation of 4'-C-methyl-2'-fluoro arabino nucleosides.

作者信息

Tiwari Kamal N, Shortnacy-Fowler Anita T, Parker William B, Waud William R, Secrist John A

机构信息

Southern Research Institute, Drug Discovery Division, Birmingham, Alabama, USA.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2009 May;28(5):657-77. doi: 10.1080/15257770903091946.

Abstract

As part of an ongoing program to develop novel antitumor agents over the years, we have synthesized and evaluated a number of 4'-C-substituted nucleosides. A few years ago, we reported the first synthesis of 4'-C-hydroxymethyl-2'-fluoro arabino nucleosides, which did not exhibit any cytotoxicity. In our exploration of related compounds, we synthesized and evaluated the 4'-C-methyl-2'-fluoro arabino nucleosides in both the purine and pyrimidine series. In the pyrimidine series, 1-(4-C-methyl-2-fluoro-beta-D-arabinofuranosyl) cytosine (13) was found to be highly cytotoxic and had significant antitumor activity in mice implanted with human tumor xenografts. The synthesis and anticancer activity of this series of nucleosides are reported.

摘要

作为多年来开发新型抗肿瘤药物的一项持续进行的计划的一部分,我们合成并评估了多种4'-C-取代核苷。几年前,我们报道了4'-C-羟甲基-2'-氟阿拉伯核苷的首次合成,该核苷未表现出任何细胞毒性。在对相关化合物的探索中,我们合成并评估了嘌呤和嘧啶系列中的4'-C-甲基-2'-氟阿拉伯核苷。在嘧啶系列中,发现1-(4-C-甲基-2-氟-β-D-阿拉伯呋喃糖基)胞嘧啶(13)具有高度细胞毒性,并且在植入人肿瘤异种移植物的小鼠中具有显著的抗肿瘤活性。本文报道了该系列核苷的合成及抗癌活性。

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