5-Substituted pyrimidine derivatives of conformationally locked nucleoside analogues
    1.
    发明授权
    5-Substituted pyrimidine derivatives of conformationally locked nucleoside analogues 有权
    5取代的构象锁定核苷类似物的嘧啶衍生物

    公开(公告)号:US07009050B2

    公开(公告)日:2006-03-07

    申请号:US10346762

    申请日:2003-01-15

    CPC分类号: C07D239/54 C07D239/553

    摘要: The embodiments described herein concern 5-substituted pyrimidine derivatives of conformationally locked nucleoside analogues and to the use of these derivatives as anti-viral and anti-cancer agents. The compounds are of the formula: wherein B is uracil-1-yl or cytosin-1-yl having a 5-substituent selected from halogen, alkyl, alkenyl, and alkynyl, with the proviso that where B is uracil-1-yl, the 5-substituent is not methyl. The compounds are useful in the treatment of Herpes simplex virus (HSV).

    摘要翻译: 本文描述的实施方案涉及构象锁定核苷类似物的5-取代嘧啶衍生物以及这些衍生物作为抗病毒和抗癌剂的用途。 所述化合物具有下式:其中B是尿嘧啶-1-基或具有选自卤素,烷基,烯基和炔基的5-取代基的细胞蛋白-1-基,条件是其中B是尿嘧啶-1-基, 5-取代基不是甲基。 该化合物可用于治疗单纯疱疹病毒(HSV)。