Steroid Analogues for Neuroprotection
    49.
    发明申请
    Steroid Analogues for Neuroprotection 审中-公开
    类固醇类似物用于神经保护

    公开(公告)号:US20170065615A1

    公开(公告)日:2017-03-09

    申请号:US15355416

    申请日:2016-11-18

    申请人: Emory University

    IPC分类号: A61K31/573

    CPC分类号: A61K31/573 C07J9/00

    摘要: Provided are steroid analogues functionalized with polar substituents at the C3 and/or C20 positions of the steroid ring system that exhibit improved water solubility. Also provided are pharmaceutical compositions comprising the steroid analogues and methods using the novel steroid analogues for the treatment and prevention of neurodegeneration in a patient following injury to the central nervous system.

    摘要翻译: 提供的是在类固醇环系统的C3和/或C20位置上被极性取代基官能化的类固醇类似物,其具有改善的水溶性。 还提供了包含类固醇类似物的药物组合物和使用新型类固醇类似物在中枢神经系统损伤后治疗和预防患者神经变性的方法。

    CXCR4 Antagonists for the Treatment of Medical Disorders
    50.
    发明申请
    CXCR4 Antagonists for the Treatment of Medical Disorders 审中-公开
    CXCR4治疗医疗障碍的拮抗剂

    公开(公告)号:US20160002174A1

    公开(公告)日:2016-01-07

    申请号:US14790531

    申请日:2015-07-02

    申请人: Emory University

    IPC分类号: C07D239/42 C07C51/41

    摘要: The invention provides compounds, pharmaceutical compositions and methods of use of certain compounds that are antagonists of the chemokine CXCR4 receptor for the treatment of proliferative conditions mediated by CXCR4 receptors. The compounds provided interfere with the binding of SDF1 to the receptor. These compounds are particularly useful for treating or reducing the severity of hyperproliferative diseases by inhibiting metastasis.

    摘要翻译: 本发明提供化合物,药物组合物和使用作为趋化因子CXCR4受体的拮抗剂的某些化合物用于治疗CXCR4受体介导的增殖性病症的化合物,药物组合物和方法。 所提供的化合物干扰SDF1与受体的结合。 这些化合物特别可用于通过抑制转移来治疗或降低过度增殖性疾病的严重性。