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[2-methoxy-5-(4-fluorophenyl)benzyl][(2S,3S)-2-phenylpiperidin-3-yl]amine

中文名称
——
中文别名
——
英文名称
[2-methoxy-5-(4-fluorophenyl)benzyl][(2S,3S)-2-phenylpiperidin-3-yl]amine
英文别名
(2S,3S)-N-[[5-(4-fluorophenyl)-2-methoxyphenyl]methyl]-2-phenylpiperidin-3-amine
[2-methoxy-5-(4-fluorophenyl)benzyl][(2S,3S)-2-phenylpiperidin-3-yl]amine化学式
CAS
——
化学式
C25H27FN2O
mdl
——
分子量
390.501
InChiKey
WSIZYTAHXOVFPZ-ZCYQVOJMSA-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):
    4.6
  • 重原子数:
    29
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    33.3
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • 5-Phenylbenzylamine compounds, process for their production and intermediates for their synthesis
    申请人:——
    公开号:US20040097548A1
    公开(公告)日:2004-05-20
    The present invention relates to a 5-phenylbenzylamine compound represented by the formula [1]: 1 wherein Ring A represents a phenyl group having a substituent(s), R a , R b1 and R b2 each represent hydrogen atom, a halogen atom, a lower alkyl group, a halogeno-lower alkyl group or a lower alkoxy group, R c1 represents hydrogen atom, a lower alkyl group optionally substituted by a heterocyclic group, or an acyl group, R c2 and R e each represent hydrogen atom or a lower alkyl group, R d represents hydrogen atom, a lower alkyl group or an acyl group, and R f represents a lower alkyl group or a cyclic lower alkyl group, or a pharmaceutically acceptable salt thereof, a process for preparing the same and synthetic intermediate thereof.
    本发明涉及一种由公式(1)表示的5-苯基苄胺化合物:其中环A代表具有取代基(Ra,Rb1和Rb2)的苯基;Ra,Rb1和Rb2各代表氢原子、卤素原子、较低的烷基、卤代较低的烷基或较低的烷氧基;Rc1代表氢原子、可选地被杂环基取代的较低烷基或酰基;Rc2和Re各代表氢原子或较低的烷基;Rd代表氢原子、较低的烷基或酰基;Rf代表较低的烷基或环状较低的烷基,或其药学上可接受的盐,以及其制备方法和合成中间体。
  • 5-PHENYLBENZYLAMINE COMPOUNDS, PROCESS FOR THEIR PRODUCTION AND INTERMEDIATES FOR THEIR SYNTHESIS
    申请人:TANABE SEIYAKU CO., LTD.
    公开号:EP1323713A1
    公开(公告)日:2003-07-02
    The present invention relates to a 5-phenylbenzylamine compound represented by the formula [1]: wherein Ring A represents a phenyl group having a substituent(s),    Ra, Rb1 and Rb2 each represent hydrogen atom, a halogen atom, a lower alkyl group, a halogeno-lower alkyl group or a lower alkoxy group,    Rc1 represents hydrogen atom, a lower alkyl group optionally substituted by a heterocyclic group, or an acyl group,    Rc2 and Re each represent hydrogen atom or a lower alkyl group,    Rd represents hydrogen atom, a lower alkyl group or an acyl group, and    Rf represents a lower alkyl group or a cyclic lower alkyl group, or a pharmaceutically acceptable salt thereof, a process for preparing the same and synthetic intermediate thereof.
    本发明涉及一种由式[1]表示的 5-苯基苄胺化合物: 其中环 A 代表具有取代基的苯基、 Ra、Rb1 和 Rb2 各自代表氢原子、卤素原子、低级烷基、卤素-低级烷基或低级烷氧基、 Rc1 代表氢原子、任选被杂环基取代的低级烷基或酰基、 Rc2 和 Re 分别代表氢原子或低级烷基、 Rd 代表氢原子、低级烷基或酰基,以及 Rf 代表低级烷基或环状低级烷基、 或其药学上可接受的盐、制备方法及其合成中间体。
  • TREATMENT OF CORNEAL NEOVASCULARIZATION
    申请人:IRBM SCIENCE PARK S.p.A.
    公开号:US20180021327A1
    公开(公告)日:2018-01-25
    There is provided inter alia a compound which is an NK-1 receptor antagonist for use in the treatment or prevention of CNV. There is also provided a compound which is an NK-1 antagonist for use in the treatment of chemical burns of the eye particularly alkali burns of the eye. There is also provided a pharmaceutical composition for topical administration to the eye comprising an NK-1 antagonist and an antibiotic agent.
  • NK-1 ANTAGONISTS FOR USE IN THE TREATMENT OF OCULAR PAIN
    申请人:OSPEDALE SAN RAFFAELE S.R.L.
    公开号:US20210015834A1
    公开(公告)日:2021-01-21
    The invention relates to compounds, in particular NK-1 antagonists, for use in the treatment of ocular sensitivity and/or ocular pain.
  • US7067535B2
    申请人:——
    公开号:US7067535B2
    公开(公告)日:2006-06-27
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