INHIBITORS OF CYCLIN DEPENDENT KINASES AND THEIR USE
    1.
    发明申请
    INHIBITORS OF CYCLIN DEPENDENT KINASES AND THEIR USE 有权
    CYCLIN依赖性激素的抑制剂及其使用

    公开(公告)号:US20070015802A1

    公开(公告)日:2007-01-18

    申请号:US11530272

    申请日:2006-09-08

    CPC分类号: C07D405/04 C07D405/14

    摘要: The present invention relates to novel compounds for the inhibition of cyclin-dependent kinases, and more particularly, to chromenone derivatives of formula (Ic) wherein R1, R2, R3, R4, R5, R6, R7 and A have the meanings indicated in the claims. The invention also relates to processes for the preparation of the compounds of formula (Ia), to methods of inhibiting cyclin-dependent kinases and of inhibiting cell proliferation, to the use of the compounds of formula (Ic) in the treatment and prophylaxis of diseases, which can be treated or prevented by the inhibition of cyclin-dependent kinases such as cancer, to the use of the compounds of formula (Ic) in the preparation of medicaments to be applied in such diseases. The invention further relates to compositions containing a compound of formula (Ic) either alone or in combination with another active agent, in admixture or otherwise in association with an inert carrier, in particular pharmaceutical compositions containing a compound of formula (Ic) either alone or in combination with another active agent, together with pharmaceutically acceptable carrier substances and auxiliary substances.

    摘要翻译: 本发明涉及用于抑制细胞周期蛋白依赖性激酶的新化合物,更具体地说,涉及其中R 1,R 2,R 2, R 3,R 4,R 5,R 6,R 7和A 具有权利要求中所示的含义。 本发明还涉及制备式(Ia)化合物的方法,抑制细胞周期蛋白依赖性激酶和抑制细胞增殖的方法,使用式(Ic)化合物在治疗和预防疾病中的用途 ,其可以通过抑制细胞周期蛋白依赖性激酶(例如癌症)来治疗或预防使用式(Ic)化合物在制备用于这些疾病的药物中的用途。 本发明还涉及含有式(Ic)化合物的组合物,其单独或与另一种活性剂组合,与惰性载体混合或以其它方式结合,特别是含有式(Ic)化合物的药物组合物,其单独或 与另一种活性剂,药学上可接受的载体物质和辅助物质一起使用。

    INHIBITORS OF CYCLIN DEPENDENT KINASES AND THEIR USE
    2.
    发明申请
    INHIBITORS OF CYCLIN DEPENDENT KINASES AND THEIR USE 有权
    CYCLIN依赖性激素的抑制剂及其使用

    公开(公告)号:US20080108690A1

    公开(公告)日:2008-05-08

    申请号:US11779577

    申请日:2007-07-18

    摘要: The present invention relates to novel compounds for the inhibition of cyclin-dependent kinases, and more particularly, to chromenone derivatives of formula (Ia), wherein R1, R2, R3, R4, R5, R6, R7 and A have the meanings indicated in the claims. The invention also relates to processes for the preparation of the compounds of formula (Ia), to methods of inhibiting cyclin-dependent kinases and of inhibiting cell proliferation, to the use of the compounds of formula (Ia) in the treatment and prophylaxis of diseases, which can be treated or prevented by the inhibition of cyclin-dependent kinases such as cancer, to the use of the compounds of formula (Ia) in the preparation of medicaments to be applied in such diseases. The invention further relates to compositions containing a compound of formula (Ia) either alone or in combination with another active agent, in admixture or otherwise in association with an inert carrier, in particular pharmaceutical compositions containing a compound of formula (Ia) either alone or in combination with another active agent, together with pharmaceutically acceptable carrier substances and auxiliary substances.

    摘要翻译: 本发明涉及用于抑制细胞周期蛋白依赖性激酶的新化合物,更具体地涉及式(Ia)的色烯酮衍生物,其中R 1,R 2, R 3,R 4,R 5,R 6,R 7和R 7, A具有权利要求中所示的含义。 本发明还涉及制备式(Ia)化合物的方法,抑制细胞周期蛋白依赖性激酶和抑制细胞增殖的方法,以使用式(Ia)化合物在治疗和预防疾病中的用途 ,其可以通过抑制细胞周期蛋白依赖性激酶(例如癌症)来治疗或预防使用式(Ia)化合物在制备用于这些疾病的药物中的用途。 本发明还涉及含有式(Ia)化合物的组合物,其单独或与另一种活性剂组合,与惰性载体混合或以其它方式结合,特别是含有式(Ia)化合物的药物组合物,其单独或 与另一种活性剂,药学上可接受的载体物质和辅助物质一起使用。