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天冬氨酸和半胱氨酸衍生物激活的pdCpA和转运RNA的合成。

Synthesis of pdCpAs and transfer RNAs activated with derivatives of aspartic acid and cysteine.

作者信息

Chen Shengxi, Hecht Sidney M

机构信息

Departments of Chemistry and Biology, University of Virginia, McCormick Road, Charlottesville, VA 22904, USA.

出版信息

Bioorg Med Chem. 2008 Oct 1;16(19):9023-31. doi: 10.1016/j.bmc.2008.08.036. Epub 2008 Aug 22.

Abstract

Described herein is the preparation of new aminoacylated derivatives of the dinucleotide pdCpA, and of transfer RNAs. The focus of the present work is the synthesis of amino acid analogs related to aspartic acid and cysteine species that have important functional roles in many proteins. The activated aminoacyl-tRNAs prepared can be utilized for the elaboration of proteins containing modified aspartic acid and cysteine derivatives at predetermined sites. Of particular interest is definition of functional group protection strategies that can be used for the preparation of the aminoacylated pdCpAs and tRNAs.

摘要

本文描述了二核苷酸pdCpA和转运RNA的新型氨酰化衍生物的制备。当前工作的重点是合成与天冬氨酸和半胱氨酸种类相关的氨基酸类似物,这些氨基酸类似物在许多蛋白质中具有重要的功能作用。所制备的活化氨酰-tRNA可用于在预定位点构建含有修饰天冬氨酸和半胱氨酸衍生物的蛋白质。特别令人感兴趣的是可用于制备氨酰化pdCpA和tRNA的官能团保护策略的定义。

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