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(2S,3S)-N-(5-ethyl-2-methoxyphenyl)methyl-2-diphenyl-methyl-1-azabicyclo[2.2.2]octan-3-amine | 147116-65-2

中文名称
——
中文别名
——
英文名称
(2S,3S)-N-(5-ethyl-2-methoxyphenyl)methyl-2-diphenyl-methyl-1-azabicyclo[2.2.2]octan-3-amine
英文别名
(2S,3S)-2-(Diphenylmethyl)-N-[(5-ethyl-2-methoxyphenyl)methyl]-1-azabicyclo[2.2.2]octan-3-amine;(2S,3S)-2-benzhydryl-N-[(5-ethyl-2-methoxyphenyl)methyl]-1-azabicyclo[2.2.2]octan-3-amine
(2S,3S)-N-(5-ethyl-2-methoxyphenyl)methyl-2-diphenyl-methyl-1-azabicyclo[2.2.2]octan-3-amine化学式
CAS
147116-65-2
化学式
C30H36N2O
mdl
——
分子量
440.629
InChiKey
MUYMQIJSHACKFJ-KYJUHHDHSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.2
  • 重原子数:
    33
  • 可旋转键数:
    8
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    24.5
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Pharmaceutical uses for fluoroalkoxybenzylamino derivatives of nitrogen containing heterocycles
    申请人:——
    公开号:US20020035147A1
    公开(公告)日:2002-03-21
    The present invention relates to methods of treating various CNS and other disorders by adminstering fluoroalkoxybenzylamino derivatives of nitrogen containing heterocyclic compounds, and specifically, by administering compounds of the formula 1 wherein Q, X 1 , X 2 and X 3 are as defined below, and their pharmaceutically acceptable salts.
    本发明涉及通过给予含氮杂环化合物的氟烷氧基苄胺生物来治疗各种中枢神经系统和其他疾病的方法,具体地,通过给予以下公式中的化合物来治疗: 1 其中Q、X 1 、X 2 和X 3 如下所定义,并且它们的药用盐。
  • [EN] QUINOLINE DERIVATIVES<br/>[FR] DERIVES QUINOLINIQUES
    申请人:PFIZER PROD INC
    公开号:WO2004043929A1
    公开(公告)日:2004-05-27
    The present invention relates to compounds of Formula I, wherein R1, R2, R3, R4, and n are as defined, and to pharmaceutically acceptable salts of said compounds. Compounds of Formula I have activity in agonizing 5HT7 receptors and are useful in treating, for example, disorders that can be treated by modulating circadian rhythms.
    本发明涉及式I的化合物,其中R1、R2、R3、R4和n如定义所述,并且涉及所述化合物的药用可接受的盐。式I的化合物在激活5HT7受体方面具有活性,并且可用于治疗例如可以通过调节昼夜节律来治疗的疾病。
  • 5HT7 Antagonists and inverse agonists
    申请人:Pfizer Inc.
    公开号:US20040229874A1
    公开(公告)日:2004-11-18
    The present invention relates to compounds of formula I, 1 and the pharmaceutically acceptable salts thereof. These compounds are useful as psychotherapeutic agents.
    本发明涉及公式I的化合物及其药用盐。这些化合物可用作心理治疗药物。
  • New pharmaceutical combinations for NOS inhibitors
    申请人:Pfizer Inc
    公开号:US20040229911A1
    公开(公告)日:2004-11-18
    The present invention relates to new pharmaceutical uses for compounds that exhibit activity as nitric oxide synthase (NOS) inhibitors. Specifically, it relates to the use of NOS inhibitors, particularly selective neuronal NOS (nNOS) inhibitors, alone or in combination with another active agent, in particular, either an SSRI or an NK-1 receptor antagonist, for the treatment of disorders or conditions the treatment which can be effected or facilitated by altering circadian rhythms. Examples of such disorders and conditions are blindness, obesity, seasonal affective disorder, bipolar disorder; jet lag, circadian sleep rhythms disorder, sleep deprivation, parasomnias, REM sleep disorders, hypersomnia, sleep-wake cycle disorders, narcolepsy and sleep disorders associated with shift work or irregular work schedules; nocturnal enuresis, and restless-legs syndrome.
    本发明涉及表现为一氧化氮合酶(NOS)抑制剂活性的化合物的新药物用途。具体地,涉及使用NOS抑制剂,特别是选择性神经元NOS(nNOS)抑制剂,单独或与另一种活性剂联合使用,特别是SSRI或NK-1受体拮抗剂,用于治疗可以通过改变昼夜节律来达到或促进治疗的疾病或病况。这些疾病和病况的例子包括失明、肥胖症、季节性情感障碍、双相情感障碍、时差反应、昼夜节律睡眠障碍、睡眠剥夺、睡眠障碍、REM睡眠障碍、嗜睡症、睡眠-觉醒周期障碍、嗜睡症和与轮班工作或不规则工作时间表相关的睡眠障碍、夜尿症和不宁腿综合症。
  • [EN] NEW PHARMACEUTICAL COMBINATIONS FOR NOS INHIBITORS<br/>[FR] NOUVELLES COMBINAISONS PHARMACEUTIQUES POUR LES INHIBITEURS DE NOS
    申请人:PFIZER PROD INC
    公开号:WO2000071107A2
    公开(公告)日:2000-11-30
    The present invention relates to new pharmaceutical uses for compounds that exhibit activity as nitric oxide synthase (NOS) inhibitors. Specifically, it relates to the use of NOS inhibitors, particularly selective neuronal NOS (nNOS) inhibitors, alone or in combination with another active agent, in particular, either an SSRI or an NK-1 receptor antagonist, for the treatment of disorders or conditions the treatment which can be effected or facilitated by altering circadian rhythms. Examples of such disorders and conditions are blindness, obesity, seasonal affective disorder, bipolar disorder, jet lag, circadian sleep rhythms disorder, sleep deprivation, parasomnias, REM sleep disorders, hypersomnia, sleep-wake cycle disorders, narcolepsy and sleep disorders associated with shift work or irregular work schedules; nocturnal enuresis, and restless-legs syndrome.
    本发明涉及表现为一氧化氮合酶(NOS)抑制剂的化合物的新药物用途。具体而言,涉及使用NOS抑制剂,特别是选择性神经元NOS(nNOS)抑制剂,单独或与另一活性剂,特别是SSRI或NK-1受体拮抗剂结合使用,治疗可以通过改变昼夜节律来实现或促进的疾病或状况。这些疾病和状况的例子包括失明,肥胖症,季节性情感障碍,双相情感障碍,时差反应,昼夜节律睡眠障碍,睡眠剥夺,睡眠障碍,REM睡眠障碍,嗜睡症,睡眠-清醒周期障碍,嗜睡症和与轮班或不规则工作时间表相关的睡眠障碍;夜尿症和不安腿综合症。
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