Isothiazoloanthrones, isoxazoloanthrones, isoindolanthrones and derivatives thereof a JNK inhibitors and compositions and methods related thereto
    1.
    发明授权
    Isothiazoloanthrones, isoxazoloanthrones, isoindolanthrones and derivatives thereof a JNK inhibitors and compositions and methods related thereto 失效
    异噻唑烷酮,异恶唑酮,异吲哚酮及其衍生物,JNK抑制剂及其组合物和方法

    公开(公告)号:US07354947B2

    公开(公告)日:2008-04-08

    申请号:US11159592

    申请日:2005-06-22

    IPC分类号: A61K31/403 C07D209/80

    CPC分类号: C07D275/04 C07D417/12

    摘要: Isaothiazoloanthrones, isooxazoloanthrones, isoindolanthrones, and derivatives thereof having the general formula: and pharmaceutically acceptable salts thereof, wherein R0 is —CH2—, —SO—, —O—, —SO2—, or —S—; compositions comprising the iazoloanthrones, isooxazoloanthrones, isoindolanthrones, and derivatives thereof; and methods for treating or preventing a disorder alleviated by inhibiting Jun N-terminal kinase (JNK) by administering the isaothiazoloanthrones, isooxazoloanthrones, isoindolanthrones, and derivatives thereof are described herein.

    摘要翻译: 异噻唑鎓,异恶唑酮,异吲哚酮及其衍生物及其药学上可接受的盐,其中R 0为-CH 2 - , - SO - , - O- ,-SO 2 - , - 或-S-; 包含重氮芳烃,异恶唑酮,异吲哚酮及其衍生物的组合物; 本文描述了通过给予异噻唑酮,异恶唑酮,异吲哚酮及其衍生物来抑制Jun N末端激酶(JNK)减轻的疾病的治疗或预防方法。

    Isothiazoloanthrones, isoxazoloanthrones, isoindolanthrones and derivatives thereof as JNK inhibitors and compositions and methods related
    2.
    发明授权
    Isothiazoloanthrones, isoxazoloanthrones, isoindolanthrones and derivatives thereof as JNK inhibitors and compositions and methods related 失效
    异噻唑烷酮,异恶唑酮,异吲哚酮及其衍生物作为JNK抑制剂及其组合物和方法相关

    公开(公告)号:US06987184B2

    公开(公告)日:2006-01-17

    申请号:US10071390

    申请日:2002-02-07

    IPC分类号: C07D417/00 C07D275/04

    CPC分类号: C07D275/04 C07D417/12

    摘要: Isothiazoloanthrones, isooxazoloanthrones, isoindolanthrones, and derivatives thereof having the general formula: and pharmaceutically acceptable salts thereof, wherein R0 is —CH2—, —SO—, —O—, —SO2—, or —S—; compositions comprising the isothiazoloanthrones, isooxazoloanthrones, isoindolanthrones, and derivatives thereof; and methods for treating or preventing a disorder alleviated by inhibiting Jun N-terminal kinase (JNK) by administering the isothiazoloanthrones, isooxazoloanthrones, isoindolanthrones, and derivatives thereof are described herein.

    摘要翻译: 异噻唑烷酮,异恶唑酮,异吲哚酮及其衍生物及其药学上可接受的盐,其中R 0为-CH 2 - , - SO - , - O- ,-SO 2 - 或-S-; 包含异噻唑烷,异恶唑酮,异吲哚酮及其衍生物的组合物; 本文描述了通过施用异噻唑酮,异恶唑酮,异吲哚酮及其衍生物来抑制Jun N末端激酶(JNK)减轻的病症的治疗或预防方法。

    PNS cell lines and methods of use therefor
    4.
    发明授权
    PNS cell lines and methods of use therefor 失效
    PNS细胞系及其使用方法

    公开(公告)号:US06835567B1

    公开(公告)日:2004-12-28

    申请号:US09060409

    申请日:1998-04-14

    IPC分类号: C12N500

    摘要: Conditionally-immortalized PNS progenitor cell lines are provided. Such cell lines, which may be clonal, may be used to generate neurons. The cell lines and/or differentiated cells may be used for the development of therapeutic agents to prevent and treat a variety of PNS-related diseases. The cell lines and/or differentiated cells may also be used in assays and for the general study of PNS cell development, death and abnormalities.

    摘要翻译: 提供有条件永生化的PNS祖细胞系。 可以使用克隆的这种细胞系来产生神经元。 细胞系和/或分化细胞可用于开发治疗剂以预防和治疗各种PNS相关疾病。 细胞系和/或分化细胞也可用于测定和PNS细胞发育,死亡和异常的一般研究。