Treatment of CNS Disorders With trans 4-(3,4-Dichlorophenyl)-1,2,3,4-Tetrahydro-1-Napthalenamine
    72.
    发明申请
    Treatment of CNS Disorders With trans 4-(3,4-Dichlorophenyl)-1,2,3,4-Tetrahydro-1-Napthalenamine 有权
    用反式4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺处理中枢神经系统疾病

    公开(公告)号:US20080280993A1

    公开(公告)日:2008-11-13

    申请号:US12173626

    申请日:2008-07-15

    IPC分类号: A61K31/136 A61P25/28

    摘要: Treatment of CNS disorders with (1R,4S)-trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine; and (1S,4R)-trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine is disclosed. A process for preparing 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine is also disclosed. The process includes the preparation of all four isomers of N-[4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl]formamide, which are also useful.

    摘要翻译: 用(1R,4S) - 反式-4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺处理CNS病症; 和(1S,4R) - 反式-4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺。 还公开了制备4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺的方法。 该方法包括制备N- [4-(3,4-二氯苯基)-1,2,3,4-四氢萘-1-基]甲酰胺的全部四种异构体,它们也是有用的。

    Peptidomimetic ligands for cellular receptors and ion channels
    73.
    发明授权
    Peptidomimetic ligands for cellular receptors and ion channels 有权
    肽模拟配体的细胞受体和离子通道

    公开(公告)号:US07446115B2

    公开(公告)日:2008-11-04

    申请号:US11512056

    申请日:2006-08-29

    摘要: One aspect of the present invention relates to novel peptidomometic compounds. A second aspect of the present invention relates to the use of the novel peptidomimetic compounds as ligands—agonists or antagonists—for various cellular receptors, e.g., G-protein-coupled receptors and opioid receptors, and various cellular ion channels, e.g., sodium and calcium. In certain embodiments, compounds of the present invention preferentially or selectively inhibit sodium or calcium ion channels. In certain embodiments, compounds of the present invention preferentially or selectively agonize or antagonize μ opioid receptors. In certain embodiments, compounds of the present invention preferentially or selectively inhibit sodium or calcium ion channels and agonize or antagonize μ-opioid receptors.

    摘要翻译: 本发明的一个方面涉及新颖的肽模拟化合物。 本发明的第二方面涉及新型拟肽化合物作为配体 - 激动剂或拮抗剂 - 用于各种细胞受体,例如G-蛋白偶联受体和阿片受体,以及各种细胞离子通道(例如钠和 钙。 在某些实施方案中,本发明的化合物优选或选择性地抑制钠离子或钙离子通道。 在某些实施方案中,本发明的化合物优选地或选择性地激动或拮抗μ阿片受体。 在某些实施方案中,本发明的化合物优选地或选择性地抑制钠离子通道或钙离子通道并且激动或拮抗μ-阿片受体。

    Treatment of CNS disorders with trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine
    76.
    发明授权
    Treatment of CNS disorders with trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine 有权
    用反式4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺处理CNS病症

    公开(公告)号:US07423179B2

    公开(公告)日:2008-09-09

    申请号:US11416586

    申请日:2006-05-03

    IPC分类号: C07C211/42

    摘要: Treatment of CNS disorders with (1R,4S)-trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine; and (1S,4R)-trans 4-(3,4-dichlorophenyl)- 1,2,3,4-tetrahydro-1-napthalenamine is disclosed. A process for preparing 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine is also disclosed. The process includes the preparation of all four isomers of N-[4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl]formamide, which are also useful.

    摘要翻译: 用(1R,4S) - 反式-4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺处理CNS病症; 和(1S,4R) - 反式-4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺。 还公开了制备4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺的方法。 该方法包括制备N- [4-(3,4-二氯苯基)-1,2,3,4-四氢萘-1-基]甲酰胺的全部四种异构体,它们也是有用的。