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N-[2-(4-chlorophenyl)-4-methylpentyl]-4-methyl-1-pyrimidin-2-yl-1H-indole-3-carboxamide | 1119281-78-5

中文名称
——
中文别名
——
英文名称
N-[2-(4-chlorophenyl)-4-methylpentyl]-4-methyl-1-pyrimidin-2-yl-1H-indole-3-carboxamide
英文别名
N-[2-(4-chlorophenyl)-4-methylpentyl]-4-methyl-1-pyrimidin-2-ylindole-3-carboxamide
N-[2-(4-chlorophenyl)-4-methylpentyl]-4-methyl-1-pyrimidin-2-yl-1H-indole-3-carboxamide化学式
CAS
1119281-78-5
化学式
C26H27ClN4O
mdl
——
分子量
446.98
InChiKey
SUYBFJWMWRJOCU-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):
    6
  • 重原子数:
    32
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    59.8
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • [EN] HETEROARYL AMIDE ANALOGUES<br/>[FR] ANALOGUES D'HÉTÉROARYLAMIDES
    申请人:NEUROGEN CORP
    公开号:WO2009023623A1
    公开(公告)日:2009-02-19
    Compounds, pharmaceutical compositions, and methods of use are disclosed for heteroaryl amide analogues of formula Ia and/or Ib: . In certain embodiments, the heteroaryl amide analogues are agonists and/or ligands of dopamine receptors and may be useful, inter alia, for the treatment of a condition responsive to P2X7 receptor modulation, for example, pain, inflammation, a neurological or neurodegenerative disorder, a cardiovascular disorder, an ocular disorder or an immune system disorder.
    公开了公式Ia和/或Ib的杂环酰胺类似物的化合物、药物组合物和使用方法。在某些实施例中,这些杂环酰胺类似物是多巴胺受体的激动剂和/或配体,可能有助于治疗对P2X7受体调节敏感的疾病,例如疼痛、炎症、神经系统或神经退行性疾病、心血管疾病、眼部疾病或免疫系统疾病。
  • Heteroaryl Amide Analogues
    申请人:Bakthavatchalam Rajagopal
    公开号:US20120190680A1
    公开(公告)日:2012-07-26
    Compounds, pharmaceutical compositions, and methods of use are disclosed for heteroaryl amide analogues of formula Ia and/or Ib: In certain embodiments, the heteroaryl amide analogues are agonists and/or ligands of dopamine receptors and may be useful, inter alia, for the treatment of a condition responsive to P2X 7 receptor modulation, for example, pain, inflammation, a neurological or neurodegenerative disorder, a cardiovascular disorder, an ocular disorder or an immune system disorder.
    本发明揭示了公式Ia和/或Ib的杂环酰胺类似物的化合物、制药组合物和使用方法:在某些实施例中,杂环酰胺类似物是多巴胺受体的激动剂和/或配体,可用于治疗对P2X7受体调节有反应的疾病,例如疼痛、炎症、神经或神经退行性疾病、心血管疾病、眼部疾病或免疫系统疾病等。
  • HETEROARYL AMIDE ANALOGUES
    申请人:H. Lundbeck A/S
    公开号:EP2185560A1
    公开(公告)日:2010-05-19
  • [EN] HETEROARYL AMIDE ANALOGUES<br/>[FR] ANALOGUES D'HÉTÉROARYLAMIDE
    申请人:LUNDBECK & CO AS H
    公开号:WO2009108551A2
    公开(公告)日:2009-09-03
    Compounds, pharmaceutical compositions, and methods of use are disclosed for heteroaryl amide analogues of formula Ia and/or Ib. In certain embodiments, the heteroaryl amide analogues are agonists and/or ligands of dopamine receptors and may be useful, inter alia, for the treatment of a condition responsive to P2X7 receptor modulation, for example, pain, inflammation, a neurological or neurodegenerative disorder, a cardiovascular disorder, an ocular disorder or an immune system disorder.
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