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    • 17. 发明申请
    • NOVEL SUBSTITUTED INDOLO 4,3 FG QUINOLINES USEFUL FOR TREATING MIGRAINE
    • 新的替代印度4,3 FG金刚石用于处理MIGRAINE
    • US20140194435A1
    • 2014-07-10
    • US14202875
    • 2014-03-10
    • MAP Pharmaceuticals, Inc.
    • Robert O. COOKThomas A. ARMERSergey Alexandrovich KOSAREVDejian XIEJian ZHANG
    • C07D457/04C07D519/02
    • C07D519/02C07D457/04
    • Provided herein are novel ergoline derivatives and pharmaceutical compositions thereof. In other embodiments, provided herein are methods of treatment, prevention, or amelioration of a variety of medical disorders such as, for example, migraine using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of agonizing receptors such as, for example, the 5-HT1D and or 5-HT1B receptor using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of antagonizing or inhibiting activity at receptors such as, for example, the 5-HT2B receptor using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of regulating serotonin transport using the compounds and compositions disclosed herein.
    • 本文提供了新的麦角灵衍生物及其药物组合物。 在其它实施方案中,本文提供了使用本文公开的化合物和组合物治疗,预防或改善各种医学病症例如偏头痛的方法。 在其它实施方案中,本文提供了使用本文公开的化合物和组合物来激发受体例如5-HT1D和/或5-HT1B受体的方法。 在其它实施方案中,本文提供了使用本文公开的化合物和组合物拮抗或抑制受体例如5-HT 2B受体的活性的方法。 在其它实施方案中,本文提供了使用本文公开的化合物和组合物调节5-羟色胺转运的方法。
    • 18. 发明授权
    • Iso-ergoline derivatives
    • 异麦角灵衍生物
    • US08722699B2
    • 2014-05-13
    • US14045767
    • 2013-10-03
    • Map Pharmaceuticals, Inc.
    • Jian ZhangRobert O. Cook
    • A01N43/42A61K31/44
    • C07D457/12C07D519/00C07D519/02
    • Provided herein are novel iso-ergoline derivatives and compositions thereof. In other embodiments, provided herein are methods of treatment, prevention, or amelioration of a variety of medical disorders such as, for example, migraine using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of agonizing receptors such as, for example, the 5-HT1D and/or the 5-HT1B receptor, without agonizing the 5-HT2B receptor using the compounds and compositions disclosed herein. In still other embodiments, provided herein are methods of antagonizing or inhibiting activity at receptors such as, for example, the adrenergic alpha2A and/or the alpha2B receptors using the compounds and compositions disclosed herein.
    • 本文提供新颖的异麦角灵衍生物及其组合物。 在其它实施方案中,本文提供了使用本文公开的化合物和组合物治疗,预防或改善各种医学病症例如偏头痛的方法。 在其它实施方案中,本文提供的是使用本文公开的化合物和组合物来激发受体例如5-HT1D和/或5-HT1B受体而不激发5-HT 2B受体的方法。 在其它实施方案中,本文提供了使用本文公开的化合物和组合物来拮抗或抑制受体例如肾上腺素α2A和/或α2B受体的活性的方法。