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2-[[2-(3-Fluorophenyl)imidazol-1-yl]methyl]-5-methyl-3-propylpyrazolo[1,5-a]pyrimidine

中文名称
——
中文别名
——
英文名称
2-[[2-(3-Fluorophenyl)imidazol-1-yl]methyl]-5-methyl-3-propylpyrazolo[1,5-a]pyrimidine
英文别名
——
2-[[2-(3-Fluorophenyl)imidazol-1-yl]methyl]-5-methyl-3-propylpyrazolo[1,5-a]pyrimidine化学式
CAS
——
化学式
C20H20FN5
mdl
——
分子量
349.4
InChiKey
SCWJQOVPINJXKR-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):
    3.5
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    48
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • Heteroaryl substituted fused bicyclic heteroaryl compounds as GABAA receptor ligands
    申请人:Hutchison Alan
    公开号:US20060014746A1
    公开(公告)日:2006-01-19
    This invention relates to heteroaryl substituted fused bicyclic heteroaryl compounds, such as heteroaryl substituted imidazopyridines, imidazopyrazines, imidazopyridizines, imidazopyrimidines, and imidazothiazoles, which may be described by Formula I or Formula II: The invention is particularly related to such compounds that bind with high selectivity and high affinity to the benzodiazepine site of GABA A receptors. This invention also relates to pharmaceutical compositions comprising such compounds and to the use of such compounds in treatment of certain central nervous system (CNS) diseases. Processes for preparing compounds of Formula I and Formula II are disclosed. This invention also relates to the use of benzimidazoles, pyridylimidazoles and related bicyclic heteroaryl compounds of Formula I or Formula II in combination with one or more other CNS agents to potentiate the effects of the other CNS agents. Additionally this invention relates to the use such compounds as probes for the localization of GABA A receptors in tissue sections.
    该发明涉及杂环取代融合双环杂环化合物,例如杂环取代咪唑吡啶咪唑吡嗪咪唑吡咯咪唑嘧啶咪唑噻唑等,可由式I或式II描述:该发明特别涉及与GABAA受体的苯二氮平位点高度选择性和高亲和力结合的这种化合物。该发明还涉及包含这种化合物的药物组合物以及使用这种化合物治疗某些中枢神经系统(CNS)疾病的用途。公开了制备式I和式II化合物的方法。此外,该发明还涉及将苯并咪唑吡啶咪唑和相关的式I或式II双环杂环化合物与一个或多个其他CNS药剂联合使用以增强其他CNS药剂的效果。此外,该发明还涉及使用这些化合物作为探针来定位组织切片中的GABAA受体。
  • METHODS AND COMPOSITIONS FOR TREATING A SUBJECT FOR CENTRAL NERVOUS SYSTEM (CNS) INJURY
    申请人:The Regents of the University of California
    公开号:EP2575455A2
    公开(公告)日:2013-04-10
  • [EN] METHODS AND COMPOSITIONS FOR TREATING A SUBJECT FOR CENTRAL NERVOUS SYSTEM (CNS) INJURY<br/>[FR] PROCÉDÉS ET COMPOSITIONS POUR LE TRAITEMENT D'UN SUJET POUR UNE LÉSION DU SYSTÈME NERVEUX CENTRAL (SNC)
    申请人:UNIV CALIFORNIA
    公开号:WO2011153377A2
    公开(公告)日:2011-12-08
    Methods for treating a central nervous system (CNS) injury in a subject are provided. Aspects of the methods include administering to the subject an effective amount of gamma aminobutyric acid (GABA) receptor signaling inhibitor to treat the subject for the CNS injury. Also provided are compositions useful in embodiments of the methods. Methods and compositions of the invention find use in the treatment of a variety of different CNS injuries, including but not limited to, treating a subject for CNS injury associated with the occurrence of stroke.
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