Anti-HIV active naphthyl analogues of HEPT and DABO.

K Danel, C Nielsen, E B Pedersen
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引用次数: 0

Abstract

5-Ethyl-6-(1-naphthylmethyl)uracil and 5-ethyl-6-(1-naphthylmethyl)-2-thiouracil were alkylated to give, respectively. N-1 and S2, ethoxymethyl and methylthiomethyl uracil derivatives. 5-Ethyl-6-(1-naphthylmethyl)-2-thiouracil was also S2 alkylated with methyl bromoacetate. The products showed activity against HIV-1, and the N-1 alkylated derivatives were indeed highly active.

抗hiv活性的HEPT和DABO的萘基类似物。
5-乙基-6-(1-萘甲基)尿嘧啶和5-乙基-6-(1-萘甲基)-2-硫脲嘧啶分别烷基化得到。N-1和S2,乙氧甲基和甲基硫甲基尿嘧啶衍生物。5-乙基-6-(1-萘基甲基)-2-硫脲嘧啶也与溴乙酸甲酯S2烷基化。产物具有抗HIV-1活性,且N-1烷基化衍生物具有较高的抗HIV-1活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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