PELORUSIDE ANALOGS
    3.
    发明申请
    PELORUSIDE ANALOGS 审中-公开

    公开(公告)号:WO2015079009A1

    公开(公告)日:2015-06-04

    申请号:PCT/EP2014/075903

    申请日:2014-11-28

    CPC classification number: C07D313/00 A61K31/365 A61K45/06 A61K2300/00

    Abstract: The present invention provides new therapeutic compounds for treatment of diseases caused or influenced by microtubule stability, such as proliferative diseases. The compounds are phenyl-analogs of the naturally occurring peloruside. The analogs are easier to synthesize, and hence open up the possibility to produce said compounds in large quantities for therapeutic use.

    Abstract translation: 本发明提供新的治疗化合物,用于治疗由微管稳定性引起或影响的疾病,如增殖性疾病。 这些化合物是天然存在的番茄红素的苯基 - 类似物。 类似物更容易合成,因此开放了大量生产所述化合物用于治疗用途的可能性。

    MACROCYCLIC COMPOUNDS USEFUL AS INHIBITORS OF KINASES AND HSP90
    10.
    发明申请
    MACROCYCLIC COMPOUNDS USEFUL AS INHIBITORS OF KINASES AND HSP90 审中-公开
    大环化合物作为KINASES和HSP90的抑制剂有用

    公开(公告)号:WO2008021213A1

    公开(公告)日:2008-02-21

    申请号:PCT/US2007/017754

    申请日:2007-08-10

    CPC classification number: C07D313/00 C07D407/04 C07D493/04

    Abstract: Disclosed are macrocyclic compounds of formulae I-V,which are analogs of the pochonin resorcylic acid lactones, and processes for the preparation of the compounds. The compounds disclosed are useful as inhibitors of kinases and Heat Shock Protein 90 (HSP 90). Also disclosed are pharmaceutical compositions comprising an effective kinase-inhibiting amount or an effective HSP90-inhibiting amount of the compounds and methods for the treatment of disorders that are mediated by kinases and HSP90.

    Abstract translation: 公开了式I-V的大环化合物,其为久金宁间苯二甲酸内酯的类似物,以及所述化合物的制备方法。 所公开的化合物可用作激酶抑制剂和热休克蛋白90(HSP 90)。 还公开了包含有效的激酶抑制量或有效的HSP90抑制量的化合物的药物组合物和用于治疗由激酶和HSP90介导的病症的方法。

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