DERIVATE, PREPARATION METHOD AND USE OF 10-METHOXYCAMPTOTHECINE
    1.
    发明申请
    DERIVATE, PREPARATION METHOD AND USE OF 10-METHOXYCAMPTOTHECINE 有权
    衍生物,制备方法和使用10-甲氧基角蛋白

    公开(公告)号:US20140194458A1

    公开(公告)日:2014-07-10

    申请号:US14124570

    申请日:2012-06-15

    IPC分类号: C07D491/22

    CPC分类号: C07D491/22

    摘要: Provided is a 10-methoxycamptothecine derivate of formula (1), wherein R is selected from hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl substituted C1-6 alkyl, phosphate substituted C1-6 alkyl, amino-substituted C1-6 alkyl, carboxyl substituted C1-6 alkyl, hydroxyl substituted C1-6 alkyl, and amide- substituted C1-6 alkyl; R1 is selected from hydrogen and t-butoxycarbonyl substituted amino. Also provided in the present invention are the preparation method of the derivate and the use thereof in anti-tumor drug preparation.

    摘要翻译: 提供式(1)的10-甲氧基喜树碱衍生物,其中R选自氢,C 1-6烷基,C 1-6卤代烷基,芳基取代的C 1-6烷基,磷酸酯取代的C 1-6烷基,氨基取代的C 1-6 烷基,羧基取代的C 1-6烷基,羟基取代的C 1-6烷基和酰胺取代的C 1-6烷基; R1选自氢和叔丁氧基羰基取代的氨基。 本发明还提供了其在抗肿瘤药物制备中的衍生及其用途的制备方法。

    Derivate, preparation method and use of 10-methoxycamptothecin
    2.
    发明授权
    Derivate, preparation method and use of 10-methoxycamptothecin 有权
    衍生,制备方法和使用10-甲氧基喜树碱

    公开(公告)号:US09034894B2

    公开(公告)日:2015-05-19

    申请号:US14124570

    申请日:2012-06-15

    IPC分类号: C07D491/22

    CPC分类号: C07D491/22

    摘要: Provided is a 10-methoxycamptothecine derivate of formula (1), wherein R is selected from hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl substituted C1-6 alkyl, phosphate substituted C1-6 alkyl, amino-substituted C1-6 alkyl, carboxyl substituted C1-6 alkyl, hydroxyl substituted C1-6 alkyl, and amide-substituted C1-6 alkyl; R1 is selected from hydrogen and t-butoxycarbonyl substituted amino. Also provided in the present invention are the preparation method of the derivate and the use thereof in anti-tumor drug preparation.

    摘要翻译: 提供式(1)的10-甲氧基喜树碱衍生物,其中R选自氢,C 1-6烷基,C 1-6卤代烷基,芳基取代的C 1-6烷基,磷酸酯取代的C 1-6烷基,氨基取代的C 1-6 烷基,羧基取代的C 1-6烷基,羟基取代的C 1-6烷基和酰胺取代的C 1-6烷基; R1选自氢和叔丁氧基羰基取代的氨基。 本发明还提供了其在抗肿瘤药物制备中的衍生及其用途的制备方法。