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3-(4-chlorophenoxy)-2-methyl-5-(trifluoromethyl)-1H-indole

中文名称
——
中文别名
——
英文名称
3-(4-chlorophenoxy)-2-methyl-5-(trifluoromethyl)-1H-indole
英文别名
——
3-(4-chlorophenoxy)-2-methyl-5-(trifluoromethyl)-1H-indole化学式
CAS
——
化学式
C16H11ClF3NO
mdl
——
分子量
325.718
InChiKey
BLQBEYDEDMDHOT-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):
    5.5
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    25
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    3-(4-chlorophenoxy)-2-methyl-5-(trifluoromethyl)-1H-indole 、 sodium hydroxide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 3-(4-chlorophenoxy)-2-methyl-5-(trifluoromethyl)-1H-indole-1-acetic acid
    参考文献:
    名称:
    Substituted indole-1-acetic acids as potent and selective CRTh2 antagonists—discovery of AZD1981
    摘要:
    Novel indole-3-thio-, 3-sulfonyl- and 3-oxy-aryl-1-acetic acids are reported which are potent, selective antagonists of the chemoattractant receptor-homologous expressed on Th2 lymphocytes receptor (CRTh2 or DP2). Optimization required maintenance of high CRTh2 potency whilst achieving a concomitant reduction in rates of metabolism, removal of cyp p450 inhibition and minimization of aldose reductase and aldehyde reductase activity. High quality compounds suitable for in vivo studies are highlighted, culminating in the discovery of AZD1981 (22). (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.08.124
  • 作为产物:
    描述:
    参考文献:
    名称:
    [EN] SUBSTITUTED INDOLE DERIVATIVES FOR PHARMACEUTICAL COMPOSITION FOR TREATING RESPIRATORY DISEASES
    [FR] DERIVES D'INDOLES SUBSTITUES POUR COMPOSITIONS PHARMACEUTIQUES PERMETTANT DE TRAITER LES TROUBLES RESPIRATOIRES
    摘要:
    本发明涉及一种公式(I)的取代吲哚化合物,可用作治疗呼吸系统疾病的药物化合物。
    公开号:
    WO2005019171A1
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文献信息

  • Substituted indole derivatives for pharmaceutical compositions for treating respiratory diseases
    申请人:Bonnert Victor Roger
    公开号:US20060264444A1
    公开(公告)日:2006-11-23
    The present invention relates to substituted indoles of formula (I) useful as pharmaceutical compounds for treating respiratory disorders.
    本发明涉及式(I)的取代吲哚,其作为治疗呼吸系统疾病的药物化合物有用。
  • SUBSTITUTED INDOLE DERIVATIVES FOR PHARMACEUTICAL COMPOSITION FOR TREATING RESPIRATORY DISEASES
    申请人:AstraZeneca AB
    公开号:EP1656347B1
    公开(公告)日:2010-10-13
  • US7709521B2
    申请人:——
    公开号:US7709521B2
    公开(公告)日:2010-05-04
  • Substituted indole-1-acetic acids as potent and selective CRTh2 antagonists—discovery of AZD1981
    作者:Tim Luker、Roger Bonnert、Steve Brough、Anthony R. Cook、Mark R. Dickinson、Iain Dougall、Chris Logan、Rukhsana T. Mohammed、Stuart Paine、Hitesh J. Sanganee、Carol Sargent、Jerzy A. Schmidt、Simon Teague、Stephen Thom
    DOI:10.1016/j.bmcl.2011.08.124
    日期:2011.11
    Novel indole-3-thio-, 3-sulfonyl- and 3-oxy-aryl-1-acetic acids are reported which are potent, selective antagonists of the chemoattractant receptor-homologous expressed on Th2 lymphocytes receptor (CRTh2 or DP2). Optimization required maintenance of high CRTh2 potency whilst achieving a concomitant reduction in rates of metabolism, removal of cyp p450 inhibition and minimization of aldose reductase and aldehyde reductase activity. High quality compounds suitable for in vivo studies are highlighted, culminating in the discovery of AZD1981 (22). (C) 2011 Elsevier Ltd. All rights reserved.
  • [EN] SUBSTITUTED INDOLE DERIVATIVES FOR PHARMACEUTICAL COMPOSITION FOR TREATING RESPIRATORY DISEASES<br/>[FR] DERIVES D'INDOLES SUBSTITUES POUR COMPOSITIONS PHARMACEUTIQUES PERMETTANT DE TRAITER LES TROUBLES RESPIRATOIRES
    申请人:ASTRAZENECA AB
    公开号:WO2005019171A1
    公开(公告)日:2005-03-03
    The present invention relates to substituted indoles of formula (I) useful as pharmaceutical compounds for treating respiratory disorders.
    本发明涉及一种公式(I)的取代吲哚化合物,可用作治疗呼吸系统疾病的药物化合物。
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