Mutual prodrug of amlodipine and atorvastatin
    3.
    发明授权
    Mutual prodrug of amlodipine and atorvastatin 失效
    氨氯地平和阿托伐他汀的前药

    公开(公告)号:US06737430B2

    公开(公告)日:2004-05-18

    申请号:US10000985

    申请日:2001-10-31

    IPC分类号: A61K314439

    摘要: The present invention relates to a mutual prodrug of amlodipine and atorvastatin, pharmaceutically acceptable acid addition salts thereof, pharmaceutical compositions thereof and the use of said prodrug and its salts in the manufacture of medicaments for the treatment of atherosclerosis, angina pectoris, combined hypertension and hyperlipidaemia and the management of cardiac risk.

    摘要翻译: 本发明涉及氨氯地平和阿托伐他汀的互用前药,其药学上可接受的酸加成盐,其药物组合物以及所述前药及其盐在制备用于治疗动脉粥样硬化,心绞痛,联合高血压和高脂血症的药物中的用途 和心脏风险的管理。

    Quinoxalinediones
    5.
    发明授权
    Quinoxalinediones 失效
    喹喔啉

    公开(公告)号:US06333326B1

    公开(公告)日:2001-12-25

    申请号:US09367303

    申请日:1999-08-02

    IPC分类号: C07D40114

    CPC分类号: C07D401/14

    摘要: This invention relates to 2,3(1H,4H)-quinoxalinedione derivatives which are selective antagonists of N-methyl-D-aspartate receptors. More particularly, this invention relates to 5-triazolyl-2,3(1H,4H)-quinoxalinedione derivatives and to the preparation of, compositions containing, and the uses of, such derivatives. It also relates to a method for treating acute neurodegeneration disorders and chronic neurological disorders.

    摘要翻译: 本发明涉及作为N-甲基-D-天冬氨酸受体的选择性拮抗剂的2,3(1H,4H) - 喹喔啉二酮衍生物。 更具体地说,本发明涉及5-三唑基-2,3(1H,4H) - 喹喔啉二酮衍生物及其制备方法,含有这些衍生物的用途和用途。 它还涉及治疗急性神经变性疾病和慢性神经障碍的方法。