Method and System for Unlocking a Touch Screen of a Mobile Electronic Device
    1.
    发明申请
    Method and System for Unlocking a Touch Screen of a Mobile Electronic Device 审中-公开
    解锁移动电子设备触摸屏的方法和系统

    公开(公告)号:US20160349984A1

    公开(公告)日:2016-12-01

    申请号:US15154772

    申请日:2016-05-13

    发明人: Weimin Ding

    摘要: This invention discloses a method and system that provides a user multiple options to unlock a touch screen of a mobile electronic device (e.g., a smartphone, tablet computer) by interacting with one or more unlock images displayed on the touch screen. When the user chooses one of the multiple options to unlock the touch screen, the invention unlocks the screen and causes an application corresponding to the option to perform an action. The application is selected from a plurality of applications installed on the mobile electronic device based on its location.

    摘要翻译: 本发明公开了一种方法和系统,其通过与显示在触摸屏上的一个或多个解锁图像交互来提供用户多个选项来解锁移动电子设备(例如,智能电话,平板计算机)的触摸屏。 当用户选择多个选项中的一个来解锁触摸屏时,本发明解锁屏幕并使与该选项相对应的应用执行动作。 基于其位置,从安装在移动电子设备上的多个应用中选择应用。

    DERIVATE, PREPARATION METHOD AND USE OF 10-METHOXYCAMPTOTHECINE
    2.
    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
    3.
    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。