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(3R,4S,5S,6S)-5-(5-isopropyl-2-methoxybenzylamino)-6-diphenylmethyl-1-azabicyclo [2.2.2]octane-3-carboxylic acid | 146725-78-2

中文名称
——
中文别名
——
英文名称
(3R,4S,5S,6S)-5-(5-isopropyl-2-methoxybenzylamino)-6-diphenylmethyl-1-azabicyclo [2.2.2]octane-3-carboxylic acid
英文别名
(1R,3R,4S,5S,6S)-6-(Diphenylmethyl)-5-(((2-methoxy-5-(1-methylethyl)phenyl)methyl)amino)-1-azabicyclo(2.2.2)octane-3-carboxylic acid;(3R,4S,5S,6S)-6-benzhydryl-5-[(2-methoxy-5-propan-2-ylphenyl)methylamino]-1-azabicyclo[2.2.2]octane-3-carboxylic acid
(3R,4S,5S,6S)-5-(5-isopropyl-2-methoxybenzylamino)-6-diphenylmethyl-1-azabicyclo [2.2.2]octane-3-carboxylic acid化学式
CAS
146725-78-2
化学式
C32H38N2O3
mdl
——
分子量
498.665
InChiKey
UGYNIDYASJFWTR-FXZOGHEHSA-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):
    3.4
  • 重原子数:
    37
  • 可旋转键数:
    9
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    61.8
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • Use of NK-1 receptor antagonists for the manufacture of a medicament in the treatment of symptoms of irritable bowel syndrome
    申请人:PFIZER INC.
    公开号:EP0873753A1
    公开(公告)日:1998-10-28
    The invention relates to the use of a NK-1 receptor antagonist, in particular a substance P receptor antagonist, for the manufacture of a medicament for the treatment of symptoms of irritable bowel syndrome.
    本发明涉及使用NK-1受体拮抗剂,特别是物质P受体拮抗剂,用于制造治疗肠易激综合征症状的药物。
  • NK-1 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF SYMPTOMS OF IRRITABLE BOWEL SYNDROME
    申请人:——
    公开号:US20010006972A1
    公开(公告)日:2001-07-05
    The present invention relates to a method of treating or preventing symptoms of irritable bowel syndrome in a mammal, including a human, using a compound that is an NK-1 receptor antagonist, in particular a substance P receptor antagonist.
    本发明涉及一种治疗或预防哺乳动物(包括人类)肠易激综合征症状的方法,使用一种NK-1受体拮抗剂化合物,特别是一种物质P受体拮抗剂。
  • 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。
  • Pharmaceutical agents for treatment of urinary incontinence
    申请人:PFIZER INC.
    公开号:EP0610021A1
    公开(公告)日:1994-08-10
    The present invention relates to a method of treating or preventing urinary incontinence in mammals, including humans, using certain quinuclidine derivatives, piperidine derivatives, azanorbornane derivatives and related compounds.
    本发明涉及一种利用某些喹吖啶衍生物、哌啶衍生物、氮杂环戊烷衍生物及相关化合物治疗或预防哺乳动物(包括人类)尿失禁的方法。
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