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9-(2-Methoxyphenyl)-2,2-dimethyl-5-morpholino-1,4-dihydro-2H-pyrano[4'',3'':4',5']pyrido[3',2':4,5]thieno[3,2-D]pyrimidin-8(9H)-one

中文名称
——
中文别名
——
英文名称
9-(2-Methoxyphenyl)-2,2-dimethyl-5-morpholino-1,4-dihydro-2H-pyrano[4'',3'':4',5']pyrido[3',2':4,5]thieno[3,2-D]pyrimidin-8(9H)-one
英文别名
14-(2-methoxyphenyl)-4,4-dimethyl-8-morpholin-4-yl-5-oxa-11-thia-9,14,16-triazatetracyclo[8.7.0.02,7.012,17]heptadeca-1(10),2(7),8,12(17),15-pentaen-13-one
9-(2-Methoxyphenyl)-2,2-dimethyl-5-morpholino-1,4-dihydro-2H-pyrano[4'',3'':4',5']pyrido[3',2':4,5]thieno[3,2-D]pyrimidin-8(9H)-one化学式
CAS
——
化学式
C25H26N4O4S
mdl
MFCD03284587
分子量
478.6
InChiKey
LPWDHNXWFLZAHM-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:
    34
  • 可旋转键数:
    3
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    105
  • 氢给体数:
    0
  • 氢受体数:
    8

文献信息

  • mGluR1 Antagonists as therapeutic agents
    申请人:Matasi J. Julius
    公开号:US20060167029A1
    公开(公告)日:2006-07-27
    In its many embodiments, the present invention provides tricyclic compounds of formula I (wherein J 1 -J 4 , X, and R 1 -R 5 are as defined herein) useful as metabotropic glutamate receptor (mGluR) antagonists, particularly as selective metabotropic glutamate receptor 1 antagonists, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds and compositions to treat diseases associated with metabotropic glutamate receptor (e.g., mGluR1) such as, for example, pain, migraine, anxiety, urinary incontinence and neurodegenerative diseases such Alzheimer's disease.
    在许多实施方案中,本发明提供了式 I 的三环化合物(其中 J 1 -J 4 、X 和 R 1 -R 5 如本文所定义)作为代谢型谷氨酸受体(mGluR)拮抗剂,特别是作为选择性代谢型谷氨酸受体 1 拮抗剂,含有这些化合物的药物组合物,以及使用这些化合物和组合物治疗与代谢型谷氨酸受体(如 mGluR1)相关疾病(如疼痛、偏头痛、焦虑、尿失禁和神经退行性疾病,如阿尔茨海默病)的方法。
  • TRICYCLIC COMPOUNDS AND THEIR USE AS MGLUR1 ANTAGONISTS
    申请人:Schering Corporation
    公开号:EP1765829B1
    公开(公告)日:2010-07-07
  • mGluR1 Antagonists as Therapeutic Agents
    申请人:Matasi Julius J.
    公开号:US20090082336A1
    公开(公告)日:2009-03-26
    In its many embodiments, the present invention provides tricyclic compounds of formula I (wherein J 1 -J 4 , X, and R 1 -R 5 are as defined herein) useful as metabotropic glutamate receptor (mGluR) antagonists, particularly as selective metabotropic glutamate receptor 1 antagonists, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds and compositions to treat diseases associated with metabotropic glutamate receptor (e.g., mGluR1) such as, for example, pain, migraine, anxiety, urinary incontinence and neurodegenerative diseases such Alzheimer's disease.
  • mGluR1 ANTAGONISTS AS THERAPEUTIC AGENTS
    申请人:Matasi Julius J.
    公开号:US20090192178A1
    公开(公告)日:2009-07-30
    In its many embodiments, the present invention provides tricyclic compounds of formula I (wherein J 1 -J 4 , X, and R 1 -R 5 are as defined herein) useful as metabotropic glutamate receptor (mGluR) antagonists, particularly as selective metabotropic glutamate receptor 1 antagonists, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds and compositions to treat diseases associated with metabotropic glutamate receptor (e.g., mGluR1) such as, for example, pain, migraine, anxiety, urinary incontinence and neurodegenerative diseases such Alzheimer's disease.
  • US7485648B2
    申请人:——
    公开号:US7485648B2
    公开(公告)日:2009-02-03
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同类化合物

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