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通过酶促切割实现环孢素前体核苷酸的细胞内捕获。

Intracellular trapping of cycloSal-pronucleotides by enzymatic cleavage.

作者信息

Jessen H J, Tonn V, Meier C

机构信息

Department of Chemistry, Organic Chemistry, Faculty of Science, University of Hamburg, Martin-Luther-King-Platz, Hamburg, Germany.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2007;26(6-7):827-30. doi: 10.1080/15257770701503886.

DOI:10.1080/15257770701503886
PMID:18066908
Abstract

A new synthesis for cycloSal-pronucleotides bearing enzymatically cleavable triggers is presented. This trigger is introduced to trap the pronucleotide inside cells. The general concept and hydrolysis data in different media are discussed.

摘要

本文介绍了一种带有可酶切触发基团的环Sal-前体核苷酸的新合成方法。引入该触发基团以将前体核苷酸捕获在细胞内。讨论了其总体概念以及在不同介质中的水解数据。

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Intracellular trapping of cycloSal-pronucleotides by enzymatic cleavage.通过酶促切割实现环孢素前体核苷酸的细胞内捕获。
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