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9-(β-L-阿拉伯呋喃糖基)腺嘌呤的合成及生物学评价

Synthesis and biological evaluation of 9-(beta-L-arabinofuranosyl)adenine.

作者信息

Boudou V, Imbach J L, Gosselin G

机构信息

Laboratoire de Chimie Bioorganique, UMR C.N.R.S. 5625, Université de Montpellier II, Sciences et Techniques du Languedoc, France.

出版信息

Nucleosides Nucleotides. 1999 Nov-Dec;18(11-12):2463-73. doi: 10.1080/07328319908044620.

DOI:10.1080/07328319908044620
PMID:10639749
Abstract

For the first time, the stereospecific synthesis of 9-(beta-L-arabinofuranosyl) adenine was carried out. Unfortunately, and unlike its "natural" D-counterpart Vidarabine, this L-enantiomer did not show significant activity when evaluated against a broad range of viruses.

摘要

首次实现了9-(β-L-阿拉伯呋喃糖基)腺嘌呤的立体选择性合成。遗憾的是,与它的“天然”D型对应物阿糖腺苷不同,这种L型对映体在针对多种病毒进行评估时并未显示出显著活性。

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