Pyrrolidine triple reuptake inhibitors
    5.
    发明授权
    Pyrrolidine triple reuptake inhibitors 有权
    吡咯烷三重再摄取抑制剂

    公开(公告)号:US09056830B2

    公开(公告)日:2015-06-16

    申请号:US14078284

    申请日:2013-11-12

    摘要: In various embodiments, the present invention provides cycloalkyl pyrrolidine compounds and methods for their use in the treatment and/or prevention of various diseases, conditions and syndromes, including central nervous system (CNS) disorders, such as depression, anxiety, schizophrenia and sleep disorder as well as methods for their synthesis. The invention also relates to pharmaceutical compositions containing the compounds of the invention, as well as methods of inhibiting reuptake of endogenous monoamines, such as dopamine, serotonin and norepinephrine from the synaptic cleft and methods of modulating one or more monoamine transporter.

    摘要翻译: 在各种实施方案中,本发明提供环烷基吡咯烷化合物及其用于治疗和/或预防各种疾病,病症和综合征的方法,包括中枢神经系统(CNS)障碍,例如抑郁症,焦虑症,精神分裂症和睡眠障碍 以及它们的合成方法。 本发明还涉及含有本发明化合物的药物组合物,以及抑制内源性单胺如从突触间隙中再摄取多巴胺,5-羟色胺和去甲肾上腺素以及调节一种或多种单胺转运蛋白的方法。

    Pyrrolidine triple reuptake inhibitors
    8.
    发明授权
    Pyrrolidine triple reuptake inhibitors 有权
    吡咯烷三重再摄取抑制剂

    公开(公告)号:US08754117B2

    公开(公告)日:2014-06-17

    申请号:US13752086

    申请日:2013-01-28

    摘要: In various embodiments, the present invention provides cycloalkyl pyrrolidine compounds and methods for their use in the treatment and/or prevention of various diseases, conditions and syndromes, including central nervous system (CNS) disorders, such as depression, anxiety, schizophrenia and sleep disorder as well as methods for their synthesis. The invention also relates to pharmaceutical compositions containing the compounds of the invention, as well as methods of inhibiting reuptake of endogenous monoamines, such as dopamine, serotonin and norepinephrine from the synaptic cleft and methods of modulating one or more monoamine transporter.

    摘要翻译: 在各种实施方案中,本发明提供环烷基吡咯烷化合物及其用于治疗和/或预防各种疾病,病症和综合征的方法,包括中枢神经系统(CNS)障碍,例如抑郁症,焦虑症,精神分裂症和睡眠障碍 以及它们的合成方法。 本发明还涉及含有本发明化合物的药物组合物,以及抑制内源性单胺如从突触间隙中再摄取多巴胺,5-羟色胺和去甲肾上腺素以及调节一种或多种单胺转运蛋白的方法。