CASPASE INHIBITOR PRODRUGS
    41.
    发明申请

    公开(公告)号:US20110137037A1

    公开(公告)日:2011-06-09

    申请号:US12971649

    申请日:2010-12-17

    CPC classification number: C07D498/04

    Abstract: This invention relates to prodrugs of caspase inhibitors comprising of a furo[3,2-d]oxazolin-5-one moiety which, under specific conditions, can convert into biologically active compounds, particularly caspase inhibitors.This invention also relates to the processes for preparing these prodrugs of caspase inhibitors.This invention further relates to pharmaceutical compositions comprising said prodrugs and to the use thereof for the treatment of diseases related to inflammatory or degenerative conditions.

    Abstract translation: 本发明涉及包含呋喃并[3,2-d]恶唑啉-5-酮部分的胱天蛋白酶抑制剂的前体药物,其在特定条件下可转化为生物活性化合物,特别是胱天蛋白酶抑制剂。 本发明还涉及制备这些半胱天冬酶抑制剂前药的方法。 本发明还涉及包含所述前药的药物组合物及其用于治疗与炎性或退行性疾病相关的疾病的用途。

    Caspase inhibitor prodrugs
    42.
    发明授权
    Caspase inhibitor prodrugs 有权
    胱天蛋白酶抑制剂前药

    公开(公告)号:US07879891B2

    公开(公告)日:2011-02-01

    申请号:US11489939

    申请日:2006-07-20

    CPC classification number: C07D498/04

    Abstract: This invention relates to prodrugs of caspase inhibitors comprising of a furo[3,2-d]oxazolin-5-one moiety which, under specific conditions, can convert into biologically active compounds, particularly caspase inhibitors.This invention also relates to the processes for preparing these prodrugs of caspase inhibitors.This invention further relates to pharmaceutical compositions comprising said prodrugs and to the use thereof for the treatment of diseases related to inflammatory or degenerative conditions.

    Abstract translation: 本发明涉及包含呋喃并[3,2-d]恶唑啉-5-酮部分的胱天蛋白酶抑制剂的前体药物,其在特定条件下可转化为生物活性化合物,特别是胱天蛋白酶抑制剂。 本发明还涉及制备这些半胱天冬酶抑制剂前药的方法。 本发明还涉及包含所述前药的药物组合物及其用于治疗与炎性或退行性疾病相关的疾病的用途。

    Pyridones useful as inhibitors of kinases
    44.
    发明授权
    Pyridones useful as inhibitors of kinases 有权
    可用作激酶抑制剂的吡啶酮

    公开(公告)号:US07691885B2

    公开(公告)日:2010-04-06

    申请号:US11511895

    申请日:2006-08-29

    CPC classification number: C07D401/04 C07D401/12

    Abstract: The present invention relates to compounds useful as inhibitors of protein kinase. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders. The invention also provides processes for preparing compounds of the inventions.

    Abstract translation: 本发明涉及可用作蛋白激酶抑制剂的化合物。 本发明还提供包含所述化合物的药学上可接受的组合物和使用该组合物治疗各种疾病,病症或病症的方法。 本发明还提供了制备本发明化合物的方法。

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