Sensitization of cancer cells to DNA damage by inhibiting kinases essential for DNA damage checkpoint control
    1.
    发明授权
    Sensitization of cancer cells to DNA damage by inhibiting kinases essential for DNA damage checkpoint control 有权
    通过抑制DNA损伤检查点控制所必需的激酶,使癌细胞对DNA损伤的敏感

    公开(公告)号:US09421203B2

    公开(公告)日:2016-08-23

    申请号:US14564186

    申请日:2014-12-09

    CPC classification number: A61K31/496 A61K31/7068 A61K2300/00

    Abstract: The invention provides methods for overriding cell cycle arrest in a tumor cell, which comprise inducing DNA damage in the cell, and contacting the cell with an amount of bosutinib or a bosutinib isomer effective to inhibit one or more kinase constituents of a DNA damage checkpoint pathway. The invention also provides novel bosutinib isomers, as well as compositions of the novel isomers and the bosutinib isomer 3,5-dichloro-4-methoxyaniline.

    Abstract translation: 本发明提供了覆盖肿瘤细胞中的细胞周期阻滞的方法,其包括诱导细胞中的DNA损伤,并使细胞与一定量的有效抑制DNA损伤检查点通路的一个或多个激酶成分的波苏替尼或波苏替尼异构体接触 。 本发明还提供新颖的波生坦异构体,以及新异构体的组合物和bosutinib异构体3,5-二氯-4-甲氧基苯胺。

    SENSITIZATION OF CANCER CELLS TO DNA DAMAGE BY INHIBITING KINASES ESSENTIAL FOR DNA DAMAGE CHECKPOINT CONTROL
    2.
    发明申请
    SENSITIZATION OF CANCER CELLS TO DNA DAMAGE BY INHIBITING KINASES ESSENTIAL FOR DNA DAMAGE CHECKPOINT CONTROL 有权
    通过抑制动物DNA损伤检测点控制的基础,癌细胞对DNA损伤的敏感性

    公开(公告)号:US20150133466A1

    公开(公告)日:2015-05-14

    申请号:US14564186

    申请日:2014-12-09

    CPC classification number: A61K31/496 A61K31/7068 A61K2300/00

    Abstract: The invention provides methods for overriding cell cycle arrest in a tumor cell, which comprise inducing DNA damage in the cell, and contacting the cell with an amount of bosutinib or a bosutinib isomer effective to inhibit one or more kinase constituents of a DNA damage checkpoint pathway. The invention also provides novel bosutinib isomers, as well as compositions of the novel isomers and the bosutinib isomer 3,5-dichloro-4-methoxyaniline.

    Abstract translation: 本发明提供了覆盖肿瘤细胞中的细胞周期阻滞的方法,其包括诱导细胞中的DNA损伤,并使细胞与一定量的有效抑制DNA损伤检查点通路的一个或多个激酶成分的波苏替尼或波苏替尼异构体接触 。 本发明还提供新颖的波生坦异构体,以及新异构体的组合物和bosutinib异构体3,5-二氯-4-甲氧基苯胺。

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