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

V Boudou, J L Imbach, G Gosselin
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引用次数: 1

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.

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9-(β - l -阿拉伯糖脲基)腺嘌呤的合成及生物学评价。
首次进行了立体定向合成9-(β - l -阿拉伯糖脲基)腺嘌呤。不幸的是,与“天然的”d对映体阿糖腺苷不同,这种l对映体在对多种病毒进行评估时没有显示出显著的活性。
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Synthesis and antiviral studies of unsaturated analogues of isomeric dideoxynucleosides. Synthesis, cytotoxic effect and antiviral activity of 1-(beta-D-arabinofuranosyl)-5-bromo-N4-substituted cytosine and 1-(beta-D-arabinofuranosyl)-5-bromo-4-methoxypyrimidin-2(1H)-one derivatives. Intramolecular glycosylation to form 4-methoxy-2,6-dioxopyrimidine nucleosides via O6,5'-cyclonucleosides. Synthesis and biological evaluation of 9-(beta-L-arabinofuranosyl)adenine. Inhibitory potency of 5-benzyluracil, 5-phenylcytosine and 5-phenylpyrimidin-2-one nucleosides against uridine phosphorylase from mouse leukemic L1210 cells.
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