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2-(4-Methylphenoxy)-4-methylpyridin | 28369-86-0

中文名称
——
中文别名
——
英文名称
2-(4-Methylphenoxy)-4-methylpyridin
英文别名
4-methyl-2-p-tolyloxy-pyridine;4-Methyl-2-(4-methylphenoxy)pyridine
2-(4-Methylphenoxy)-4-methylpyridin化学式
CAS
28369-86-0
化学式
C13H13NO
mdl
——
分子量
199.252
InChiKey
SIFUSACAQYNFDQ-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):
    3.4
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] GLYCINE B ANTAGONISTS<br/>[FR] ANTAGONISTES DE LA GLYCINE B
    申请人:MERZ PHARMA GMBH & CO KGAA
    公开号:WO2010037533A1
    公开(公告)日:2010-04-08
    The invention relates to quinoline derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are glycine B antagonists and are therefore useful for the control and prevention of various disorders, including neurological disorders.
    该发明涉及喹啉生物及其药用盐。该发明还涉及一种制备这种化合物的方法。该发明的化合物是甘酸B拮抗剂,因此对于控制和预防各种疾病,包括神经系统疾病,非常有用。
  • GLYCINE B ANTAGONIST
    申请人:Henrich Markus
    公开号:US20110190342A1
    公开(公告)日:2011-08-04
    The invention relates to quinoline derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are glycine B antagonists and are therefore useful for the control and prevention of various disorders, including neurological disorders.
    本发明涉及喹啉生物及其药学上可接受的盐。本发明还涉及制备这种化合物的过程。本发明的化合物是甘酸B拮抗剂,因此对控制和预防各种疾病,包括神经系统疾病,非常有用。
  • 1,4-DISUBSTITUTED 3-CYANO-PYRIDONE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2-RECEPTORS
    申请人:Janssen Pharmaceuticals, Inc.
    公开号:EP1994004B1
    公开(公告)日:2012-08-01
  • 1, 4-DISUBSTITUTED 3-CYANO-PYRIDONE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2-RECEPTORS
    申请人:Imogai Hassan Julien
    公开号:US20100166655A1
    公开(公告)日:2010-07-01
    The present invention relates to novel compounds, in particular novel pyridinone derivatives according to Formula (I) wherein all radicals are defined in the application and claims. The compounds according to the invention are positive allosteric modulators of metabotropic receptors-subtype 2 (“mGluR2”) which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR2 subtype of metabotropic receptors is involved. In particular, such diseases are central nervous system disorders selected from the group of anxiety, schizophrenia, migraine, depression, and epilepsy. The invention is also directed to pharmaceutical compositions and processes to prepare such compounds and compositions, as well as to the use of such compounds for the prevention and treatment of such diseases in which mGluR2 is involved.
  • 1, 4-Disubstituted 3-Cyano-Pyridone Derivatives and Their Use As Positive Allosteric Modulators of MGLUR2-Receptors
    申请人:JANSSEN PHARMACEUTICALS, INC.
    公开号:US20140315903A1
    公开(公告)日:2014-10-23
    The present invention relates to novel compounds, in particular novel pyridinone derivatives according to Formula (I) wherein all radicals are defined in the application and claims. The compounds according to the invention are positive allosteric modulators of metabotropic receptors—subtype 2 (“mGluR2”) which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR2 subtype of metabotropic receptors is involved. In particular, such diseases are central nervous system disorders selected from the group of anxiety, schizophrenia, migraine, depression, and epilepsy. The invention is also directed to pharmaceutical compositions and processes to prepare such compounds and compositions, as well as to the use of such compounds for the prevention and treatment of such diseases in which mGluR2 is involved.
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