COMPOUNDS AND METHODS FOR MODULATION OF ESTROGEN RECEPTORS
    3.
    发明授权
    COMPOUNDS AND METHODS FOR MODULATION OF ESTROGEN RECEPTORS 有权
    化合物和方法具有调节雌激素受体

    公开(公告)号:EP1246814B1

    公开(公告)日:2005-02-16

    申请号:EP00990966.4

    申请日:2000-12-29

    CPC分类号: C07D405/12 C07D311/16

    摘要: Compounds that modulate gene expression through the estrogen receptor (ER) are disclosed having formula (I), as well as pharmaceutical compositions containing the same wherein R1, R2, R3, n and p are as defined here. In a specific embodiment, the compounds are selective modulators for ER-β over ER-α. Methods are also disclosed for modulating ER-β in cells and/or tissues expressing the same, including cells and/or tissues that preferentially express ER-β. More generally, methods for treating estrogen-related conditions are also disclosed, including conditions such as breast cancer, testicular cancer, osteoporosis, endometriosis, cardiovascular disease, hypercholesterolemia, prostatic hypertrophy, prostatic carcinomas, obesity, hot flashes, skin effects, mood swings, memory loss, urinary incontinence, hairloss, cataracts, natureal hormonal imbalances, and adverse reproductive effects associated with exposure to environmental chemicals.

    HUMAN SPINAL CORD CELL LINES AND METHODS OF USE THEREFOR
    6.
    发明公开
    HUMAN SPINAL CORD CELL LINES AND METHODS OF USE THEREFOR 审中-公开
    人类RÜCKENMARKZELLINIE及使用方法

    公开(公告)号:EP1060245A2

    公开(公告)日:2000-12-20

    申请号:EP99912239.3

    申请日:1999-03-02

    IPC分类号: C12N5/10 C12Q1/00

    摘要: Conditionally-immortalized human spinal cord cell lines are provided. Such cell lines, which may be clonal, may be used to generate neurons, including motoneurons. The cell lines and/or differentiated cells may be used for the development of therapeutic agents to prevent and treat a variety of spinal cord-related diseases and injuries. The cell lines and/or differentiated cells may also be used in assays and for the general study of spinal cord cell development and differentiation.

    ANTHRONE DERIVATIVES AND THEIR USE AS JNK INHIBITORS
    10.
    发明公开
    ANTHRONE DERIVATIVES AND THEIR USE AS JNK INHIBITORS 审中-公开
    蒽酮及其作为JNK抑制剂

    公开(公告)号:EP1363891A2

    公开(公告)日:2003-11-26

    申请号:EP02720975.8

    申请日:2002-02-13

    CPC分类号: C07D275/04 C07D417/12

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