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6-[2-isopropyl-4-(1-methyl-azetidin-3-yl-oxy)-phenyl]-pyridin-2-yl-amine | 211494-70-1

中文名称
——
中文别名
——
英文名称
6-[2-isopropyl-4-(1-methyl-azetidin-3-yl-oxy)-phenyl]-pyridin-2-yl-amine
英文别名
6-[4-(1-Methylazetidin-3-yl)oxy-2-propan-2-ylphenyl]pyridin-2-amine
6-[2-isopropyl-4-(1-methyl-azetidin-3-yl-oxy)-phenyl]-pyridin-2-yl-amine化学式
CAS
211494-70-1
化学式
C18H23N3O
mdl
——
分子量
297.4
InChiKey
NBULPXHLSKJGRI-UHFFFAOYSA-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):
    3.1
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    51.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • 2-AMINO-6-(2-SUBSTITUTED-4-PHENOXY)-SUBSTITUTED-PYRIDINES
    申请人:——
    公开号:US20010007873A1
    公开(公告)日:2001-07-12
    This present invention relates to compounds of the formula 1 wherein G, R 1 and R 2 are defined as in the specification, to pharmaceutical compositions containing them and to their use in the treatment and prevention of central nervous system and other disorders.
    这项发明涉及公式1中定义的化合物,其中G、R1和R2如规范中所定义,以及含有它们的药物组合物,以及它们在治疗和预防中枢神经系统和其他疾病中的用途。
  • [EN] LACTONE INTERMEDIATES OF NICOTINAMIDE RIBOSIDE AND NICOTINATE RIBOSIDE<br/>[FR] INTERMÉDIAIRES DE LACTONE DE NICOTINAMIDE RIBOSIDE ET DE NICOTINATE RIBOSIDE
    申请人:UNIV BELFAST
    公开号:WO2018033639A1
    公开(公告)日:2018-02-22
    The present invention is directed to lactones of the following structural formula for use as precursors of NAD, and their use as nutritional supplements.
    本发明涉及以下结构式的内酯,用作NAD的前体,并且它们的用途作为营养补充剂。
  • [EN] PREPARATION AND USE OF CRYSTALLINE BETA-D-NICOTINAMIDE RIBOSIDE<br/>[FR] PRÉPARATION ET UTILISATION DE BÊTA-D-NICOTINAMIDE RIBOSIDE CRISTALLIN
    申请人:GLAXOSMITHKLINE IP NO 2 LTD
    公开号:WO2015186068A1
    公开(公告)日:2015-12-10
    Provided herein are crystalline beta-D-nicotinamide riboside chloride compositions and methods of preparation and use thereof. Also provided are related pharmaceutical compositions and methods of use thereof. The crystalline beta-D-nicotinamide riboside chloride compositions may be used to treat a disease or disorder that would benefit from increased NAD levels including a mitochondrial disease or disorder, insulin resistance, a metabolic syndrome, diabetes, obesity, or for increasing insulin sensitivity in a subject.
    本文提供晶体质的β-D-烟酰胺核苷酸化物组合物的制备和使用方法。还提供相关的药物组合物及其使用方法。晶体质的β-D-烟酰胺核苷酸化物组合物可用于治疗需要提高NAD平的疾病或疾病,包括线粒体疾病或疾病,胰岛素抵抗,代谢综合征,糖尿病,肥胖症或用于增加受试者胰岛素敏感性。
  • 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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