Instituto de Química Médica (C.S.I.C.), Juan de la Cierva 3, 28006 Madrid, Spain.
ChemMedChem. 2011 Apr 4;6(4):686-97. doi: 10.1002/cmdc.201000546. Epub 2011 Mar 2.
Herein we describe the first successful application of the β-amino-γ-sultone system as an intermediate for the synthesis of hitherto virtually unknown 3H-[1,2]-oxathiole [4,3-b]pyridine and pyrazine 1,1-dioxide bicyclic heterocyclic systems. All novel compounds were evaluated for their antiviral and cytostatic activities. Compounds 3 a, 15 a, and 21 a inhibited HIV-1-induced cytopathicity. Compound 7 showed remarkable cytostatic activity, and can be regarded as a potential antitumor candidate for further exploration.
在此,我们首次成功应用β-氨基-γ-砜体系作为合成 hitherto 几乎未知的 3H-[1,2]-氧杂硫杂环戊烯[4,3-b]吡啶和吡嗪 1,1-二氧化物双环杂环系统的中间体。所有新型化合物均进行了抗病毒和细胞毒性活性评价。化合物 3a、15a 和 21a 抑制 HIV-1 诱导的细胞病变作用。化合物 7 表现出显著的细胞毒性活性,可作为进一步探索的潜在抗肿瘤候选药物。