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Targeting DNA

机译:靶向DNA

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摘要

The drug discovery world is protein-centric, and largely neglects nucleic acids as viable targets for new therapeutics. Nucleic acids, and especially DNA, are often perceived as being structurally monotonous, and lacking the structural diversity to offer novel "druggable" targets. This special issue of Biochimie was assembled, in part, to dispel these myths. As written before "DNA comes in many forms" [1], or, in line with a Biochimie special issue on topoisomerases published last year, DNA is "more than just a ladder" [2]. Small molecules can and do recognize DNA sequences and structures with high selectivity. Non-canonical DNA structures are emerging as important functional elements in gene expression and in telomere biology, and offer new avenues for the development of novel types of small molecule therapeutics. This issue features reviews and original research articles that highlight unique aspects of nucleic acids that make them suitable drug targets.
机译:药物发现世界是以蛋白质为中心的,并且很大程度上忽略了核酸作为新疗法的可行靶标。核酸,尤其是DNA,通常被认为在结构上是单调的,并且缺乏提供新的“可吸收”靶标的结构多样性。本期《生物化学》特刊的发行部分是为了消除这些神话。正如“ DNA有多种形式” [1]之前写的那样,或者与去年发表的有关拓扑异构酶的Biochimie特刊一致,DNA不仅仅是“一个阶梯” [2]。小分子可以并且确实以高选择性识别DNA序列和结构。非规范的DNA结构正在成为基因表达和端粒生物学中的重要功能元件,并为开发新型小分子疗法提供了新途径。本期刊载评论和原创研究文章,着重介绍使核酸成为合适药物靶标的独特方面。

著录项

  • 来源
    《Biochimie》 |2008年第7期|p.973-975|共3页
  • 作者

  • 作者单位
  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

  • 入库时间 2022-08-18 01:24:11

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