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1-[4-(1-Pyrrolidinylcarbonyl)phenyl]-3-(Trifluoromethyl)-4,5,6,7-Tetrahydro-1h-Indazole

中文名称
——
中文别名
——
英文名称
1-[4-(1-Pyrrolidinylcarbonyl)phenyl]-3-(Trifluoromethyl)-4,5,6,7-Tetrahydro-1h-Indazole
英文别名
pyrrolidin-1-yl-[4-[3-(trifluoromethyl)-4,5,6,7-tetrahydroindazol-1-yl]phenyl]methanone
1-[4-(1-Pyrrolidinylcarbonyl)phenyl]-3-(Trifluoromethyl)-4,5,6,7-Tetrahydro-1h-Indazole化学式
CAS
——
化学式
C19H20F3N3O
mdl
——
分子量
363.4
InChiKey
PMXYSSZJPIWCHI-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):
    4
  • 重原子数:
    26
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    38.1
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]benzoic acidN,N'-羰基二咪唑四氢吡咯 在 silica 、 乙酸乙酯 、 petroleum ether 作用下, 以 二氯甲烷 为溶剂, 反应 1.25h, 以to give the title compound as a yellow oil (51 mg, 50%)的产率得到1-[4-(1-Pyrrolidinylcarbonyl)phenyl]-3-(Trifluoromethyl)-4,5,6,7-Tetrahydro-1h-Indazole
    参考文献:
    名称:
    Compounds Which Potentiate AMPA Receptor and Uses Thereof in Medicine
    摘要:
    提供式(I)的化合物和盐,以及药物组合物,用于医学用途,例如治疗由谷氨酸受体功能降低或失衡所介导的疾病或病情,如精神分裂症或认知障碍。
    公开号:
    US20090118280A1
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文献信息

  • Compounds which potentiate AMPA receptor and uses thereof in medicine
    申请人:Harrison Stephen
    公开号:US20080045532A1
    公开(公告)日:2008-02-21
    Compounds of formula (I) and salts are provided: along with pharmaceutical compositions, uses in medicine, e.g., treating disease or condition mediated by a reduction or imbalance in glutamate receptor function, such as schizophrenia or cognition impairment.
    提供式(I)化合物和盐,以及药物组合物,用于医学上的用途,例如治疗由谷酸受体功能减弱或失衡引起的疾病或症状,如精神分裂症或认知障碍。
  • COMPOUNDS WHICH POTENTIATE AMPA RECEPTOR AND USES THEREOF IN MEDICINE
    申请人:GLAXO GROUP LIMITED
    公开号:EP1996555A1
    公开(公告)日:2008-12-03
  • UPREGULATING BDNF LEVELS TO MITIGATE MENTAL RETARDATION
    申请人:LAUTERBORN JULIE
    公开号:US20080139472A1
    公开(公告)日:2008-06-12
    This invention provides methods of preserving, improving, or restoring cognitive function in mammal having one or more mutations in the FMR1 gene (e.g. at risk for or having fragile x syndrome), where the methods involve the brain derived neurotrophic factor (BDNF) level or activity in the brain of said mammal. In certain embodiments the methods involve administering one or more AMPA potentiators (e.g., ampakines) to the mammal in an amount sufficient to increase BDNF levels in the brain of the mammal.
  • Modulation of AMPA/kainate Receptors for the Treatment of Hypoglycemia
    申请人:Vanderklish Peter
    公开号:US20200397751A1
    公开(公告)日:2020-12-24
    Methods for modulating the levels of glucagon and blood glucose of a mammal are provided. In the subject methods, a positive allosteric modulator of AMPA/kainate receptors is administered to a host. The subject methods find use in applications where it is desired to increase one or both of the glucagon and blood glucose levels in a mammalian host. The subject methods find use in applications where it is desired to decrease the size, or breadth, of the circadian range of blood glucose levels in a mammalian host. The subject methods also find use in applications where it is desired to decrease the frequency, severity, or occurrence of hypoglycemia in a mammalian host. Finally, the subject method finds use in applications where it is desired to decrease the frequency, severity, or occurrence of nocturnal hypoglycemia in a mammalian host, particularly that which occurs in diabetics as a result of therapy with insulins or insulin analogs or other glucose lowering agents, or combinations of such agents.
  • US7566735B2
    申请人:——
    公开号:US7566735B2
    公开(公告)日:2009-07-28
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