5HT2C receptor modulator compositions and methods of use
    1.
    发明授权
    5HT2C receptor modulator compositions and methods of use 失效
    5HT2C受体调节剂组合物和使用方法

    公开(公告)号:US08546378B2

    公开(公告)日:2013-10-01

    申请号:US13418151

    申请日:2012-03-12

    IPC分类号: A61K31/55 A61K31/50

    摘要: The present invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist. In addition, the invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist having Formula (I): or a pharmaceutically acceptable salt, solvate or hydrate thereof. These compositions are useful in pharmaceutical compositions whose use includes the treatment of obesity.

    摘要翻译: 本发明涉及包含苯丁胺和选择性5HT-2C受体激动剂的组合物。 此外,本发明涉及包含苯丁胺和具有式(I)的选择性5HT-2C受体激动剂或其药学上可接受的盐,溶剂合物或水合物的组合物。 这些组合物可用于其用途包括治疗肥胖症的药物组合物中。

    5HT2C RECEPTOR MODULATOR COMPOSITIONS
    2.
    发明申请
    5HT2C RECEPTOR MODULATOR COMPOSITIONS 审中-公开
    5HT2C受体调节剂组合物

    公开(公告)号:US20150087634A1

    公开(公告)日:2015-03-26

    申请号:US14259748

    申请日:2014-04-23

    IPC分类号: A61K31/55 A61K31/137

    摘要: The present invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist. In addition, the invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist having Formula (I): or a pharmaceutically acceptable salt, solvate or hydrate thereof. These compositions are useful in pharmaceutical compositions whose use includes the treatment of obesity.

    摘要翻译: 本发明涉及包含苯丁胺和选择性5HT-2C受体激动剂的组合物。 此外,本发明涉及包含苯丁胺和具有式(I)的选择性5HT-2C受体激动剂或其药学上可接受的盐,溶剂合物或水合物的组合物。 这些组合物可用于其用途包括治疗肥胖症的药物组合物中。

    5ht2C receptor modulator compositions
    3.
    发明授权
    5ht2C receptor modulator compositions 有权
    5ht2C受体调节剂组合物

    公开(公告)号:US08153621B2

    公开(公告)日:2012-04-10

    申请号:US11793941

    申请日:2005-12-21

    IPC分类号: A61K31/55

    摘要: The present invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist. In addition, the invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist having Formula (I): or a pharmaceutically acceptable salt, solvate or hydrate thereof. These compositions are useful in pharmaceutical compositions whose use includes the treatment of obesity.

    摘要翻译: 本发明涉及包含苯丁胺和选择性5HT-2C受体激动剂的组合物。 此外,本发明涉及包含苯丁胺和具有式(I)的选择性5HT-2C受体激动剂或其药学上可接受的盐,溶剂合物或水合物的组合物。 这些组合物可用于其用途包括治疗肥胖症的药物组合物中。

    5ht2c receptor modulator compositions and methods of use
    4.
    发明申请
    5ht2c receptor modulator compositions and methods of use 有权
    5ht2c受体调节剂组合物和使用方法

    公开(公告)号:US20090197868A1

    公开(公告)日:2009-08-06

    申请号:US11793941

    申请日:2005-12-21

    摘要: The present invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist. In addition, the invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist having Formula (I): or a pharmaceutically acceptable salt, solvate or hydrate thereof. These compositions are useful in pharmaceutical compositions whose use includes the treatment of obesity.

    摘要翻译: 本发明涉及包含苯丁胺和选择性5HT-2C受体激动剂的组合物。 此外,本发明涉及包含苯丁胺和具有式(I)的选择性5HT-2C受体激动剂或其药学上可接受的盐,溶剂合物或水合物的组合物。 这些组合物可用于其用途包括治疗肥胖症的药物组合物中。

    5HT2C RECEPTOR MODULATOR COMPOSITIONS AND METHODS OF USE
    5.
    发明申请
    5HT2C RECEPTOR MODULATOR COMPOSITIONS AND METHODS OF USE 失效
    5HT2C受体调节剂组合物及其使用方法

    公开(公告)号:US20120252786A1

    公开(公告)日:2012-10-04

    申请号:US13418151

    申请日:2012-03-12

    IPC分类号: A61K31/55 A61P3/10

    摘要: The present invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist. In addition, the invention relates to a composition comprising phentermine and a selective 5HT-2C receptor agonist having Formula (I): or a pharmaceutically acceptable salt, solvate or hydrate thereof. These compositions are useful in pharmaceutical compositions whose use includes the treatment of obesity.

    摘要翻译: 本发明涉及包含苯丁胺和选择性5HT-2C受体激动剂的组合物。 此外,本发明涉及包含苯丁胺和具有式(I)的选择性5HT-2C受体激动剂或其药学上可接受的盐,溶剂合物或水合物的组合物。 这些组合物可用于其用途包括治疗肥胖症的药物组合物中。

    Brain-derived membrane-associated CRF binding proteins
    9.
    发明授权
    Brain-derived membrane-associated CRF binding proteins 失效
    脑衍生的膜相关CRF结合蛋白

    公开(公告)号:US5910428A

    公开(公告)日:1999-06-08

    申请号:US637761

    申请日:1996-07-02

    CPC分类号: C07K14/72

    摘要: Isolated, substantially pure mammalian brain-derived membrane-associated CRF-binding proteins and biologically active fragments thereof are provided as well as isolated and purified DNA fragments which encode the CRF binding proteins or biologically active fragments thereof or homologs of other mammalian species. By administering an amount of such CRF binding protein or a fragment thereof effective to modulate receptor activation, it is possible to modulate the action of CRF upon (a) the brain and nervous system, (b) the pituitary particularly for production of ACTH, beta endorphin and cortisol, (c) sites of inflammation, (d) the placenta, (e) the adrenal glands, (f) the gonads or (g) the gastrointestinal tract. Administration of an N-terminal fragment of the protein increases the binding site density for CRF and thus modulates its biological effect in vivo.

    摘要翻译: PCT No.PCT / US94 / 12672 Sec。 371日期:1996年7月2日 102(e)日期1996年7月2日PCT 1994年11月7日PCT PCT。 公开号WO95 / 13372 日期1995年5月18日提供了分离的,基本上纯的哺乳动物脑衍生的膜相关CRF结合蛋白及其生物活性片段,以及分离和纯化的DNA片段,其编码CRF结合蛋白或其生物活性片段或其他哺乳动物的同源物 种类。 通过施用一定量的有效调节受体激活的CRF结合蛋白或其片段,有可能在(a)脑和神经系统调节CRF的作用,(b)垂体特别是用于产生ACTH,β 内啡肽和皮质醇,(c)炎症部位,(d)胎盘,(e)肾上腺,(f)性腺或(g)胃肠道。 施用蛋白质的N-末端片段增加CRF的结合位点密度,从而调节其在体内的生物学效应。