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Synthesis and antiviral activity of boranophosphonate isosteres of AZT and d4T monophosphates.

机译:AZT和d4T单磷酸硼酸膦酸酯等排体的合成及其抗病毒活性。

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摘要

We report synthesis, in vitro antiviral activity, and stability studies in biological media of original boranophosphonate isosteres of AZT and d4T monophophates. A convenient route for the synthesis of 3'-Azido-3'-deoxythymidine-5'-boranophosphonate 8 and 2',3'-Didehydro-3'-dideoxythymidine-5'-boranophosphonate 12 is described. H-phosphinates 7 and 11, and alpha-boranophosphonates 8 and 12 exhibited no significant in vitro activity against HIV-infected cells, neither against a broad panel of viruses, up to 200 microM. The absence of activity of target compounds 8 and 12 can be partially explained by their short half-life in culture medium.
机译:我们报告的合成,体外抗病毒活性,以及​​在AZT和d4T monophophates的原始硼烷膦酸酯等位基因的生物培养基中的稳定性研究。描述了合成3'-叠氮基-3'-脱氧胸苷-5'-硼膦酸酯8和2',3'-二氢加氢-3'-二脱氧胸苷-5'-硼膦酸酯12的简便方法。 H-次膦酸酯7和11,以及α-硼烷膦酸酯8和12对HIV感染的细胞没有显着的体外活性,对高达200 microM的多种病毒也没有显着的体外活性。目标化合物8和12没有活性的部分原因是它们在培养基中的半衰期短。

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