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4-(1-Methyl-1H-[1,2,3]triazol-4-ylmethoxy)-2-phenylquinoline

中文名称
——
中文别名
——
英文名称
4-(1-Methyl-1H-[1,2,3]triazol-4-ylmethoxy)-2-phenylquinoline
英文别名
4-[(1-Methyltriazol-4-yl)methoxy]-2-phenylquinoline
4-(1-Methyl-1H-[1,2,3]triazol-4-ylmethoxy)-2-phenylquinoline化学式
CAS
——
化学式
C19H16N4O
mdl
——
分子量
316.362
InChiKey
FIJZLYKCQVXHSO-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):
    3.1
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    52.8
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • Aryl fused substituted 4-oxy-pyridines
    申请人:——
    公开号:US20020035121A1
    公开(公告)日:2002-03-21
    Disclosed are compounds of the formula: 1 wherein X, Q, W and 2 are as defined herein. These compounds are agonists, antagonists or inverse agonists for GABA A brain receptors or prodrugs of agonists, antagonists or inverse agonists for GABA A brain receptors and are therefore useful in the diagnosis and treatment of anxiety, depression, Down Syndrome, sleep and seizure disorders, overdose with benzodiazepine drugs and for enhancement of memory. Pharmaceutical compositions, including packaged pharmaceutical compositions, are further provided. Compounds of the invention are also useful as probes for the localization of GABA A receptors in tissue samples.
    本发明揭示了化合物的公式:1,其中X,Q,W和2如定义所述。这些化合物是GABAA脑受体的激动剂,拮抗剂或反向激动剂,或者是GABAA脑受体激动剂,拮抗剂或反向激动剂的前药,因此在焦虑,抑郁,唐氏综合症,睡眠和癫痫障碍,苯二氮卓类药物过量和记忆增强的诊断和治疗中有用。此外,还提供了包括包装的制药组合物在内的制药组合物。本发明的化合物还可用作组织样本中GABAA受体定位的探针。
  • US6828329B2
    申请人:——
    公开号:US6828329B2
    公开(公告)日:2004-12-07
  • US7371752B2
    申请人:——
    公开号:US7371752B2
    公开(公告)日:2008-05-13
  • [EN] ARYL FUSED SUBSTITUTED 4-OXY-PYRIDINES<br/>[FR] 4-OXY-PYRIDINES SUBSTITUEES A FUSION ARYLE
    申请人:NEUROGEN CORP
    公开号:WO2002000623A2
    公开(公告)日:2002-01-03
    Disclosed are compounds of the formula (I): wherein X, Q, W and formula (II) are as defined herein. These compounds are agonists, antagonists or inverse agonists for GABAA brain receptors or prodrugs of agonists, antagonists or inverse agonists of GABAA brain receptors and are therefore useful in the diagnosis and treatment of anxiety, depression, Down Syndrome, sleep and seizure disorders, overdose with benzodiazepine drugs and for enhancement of memory. Pharmaceutical compositions, including packaged pharmaceutical compositions, are further provided. Compounds of the invention are also useful as probes for the localization of GABAA receptors in tissue samples.
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