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2-[4-(1-Methylethyl)-1-piperazinyl]-6-quinolinecarbonitrile | 577967-90-9

中文名称
——
中文别名
——
英文名称
2-[4-(1-Methylethyl)-1-piperazinyl]-6-quinolinecarbonitrile
英文别名
2-(4-propan-2-ylpiperazin-1-yl)quinoline-6-carbonitrile
2-[4-(1-Methylethyl)-1-piperazinyl]-6-quinolinecarbonitrile化学式
CAS
577967-90-9
化学式
C17H20N4
mdl
——
分子量
280.37
InChiKey
GZBQWMWZEZTKSS-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
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    43.2
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • Novel aryl- and heteroarylpiperazines
    申请人:——
    公开号:US20030236259A1
    公开(公告)日:2003-12-25
    Novel aryl- and heteroarylpiperazines, use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds, and a method of treatment employing these compounds and compositions. The compounds show a high and selective binding affinity to the histamine H3 receptor indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity. As a result, the compounds are useful for the treatment of diseases and disorders related to the histamine H3 receptor.
    新颖的芳基和杂环基哌嗪类化合物,这些化合物作为药物组合物的用途,包含这些化合物的药物组合物,以及利用这些化合物和组合物的治疗方法。这些化合物显示出对组胺H3受体的高度和选择性结合亲和力,表明具有组胺H3受体拮抗、逆激动或激动活性。因此,这些化合物对于治疗与组胺H3受体相关的疾病和紊乱是有用的。
  • Novel Aryl- and Heteroarylpiperazines
    申请人:Hohlweg Rolf
    公开号:US20090264435A1
    公开(公告)日:2009-10-22
    Novel aryl- and heteroarylpiperazines, use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds, and a method of treatment employing these compounds and compositions. The compounds show a high and selective binding affinity to the histamine H3 receptor indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity. As a result, the compounds are useful for the treatment of diseases and disorders related to the histamine H3 receptor.
    新型芳基和杂环基哌嗪,这些化合物的药用组合物,包含这些化合物的药用组合物,以及采用这些化合物和组合物的治疗方法。这些化合物表现出高度和选择性的结合亲和力,表明它们具有组胺H3受体拮抗、反向激动或激动活性。因此,这些化合物对于治疗与组胺H3受体相关的疾病和障碍非常有用。
  • NOVEL ARYL- AND HETEROARYLPIPERAZINES
    申请人:NOVO NORDISK A/S
    公开号:EP1474401A2
    公开(公告)日:2004-11-10
  • [EN] NOVEL ARYL- AND HETEROARYLPIPERAZINES<br/>[FR] NOUVELLES ARYL- ET HETEROARYLPIPERAZINES
    申请人:NOVO NORDISK AS
    公开号:WO2003066604A2
    公开(公告)日:2003-08-14
    Novel aryl- and heteroarylpiperazines, use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds, and a method of treatment employing these compounds and compositions. The compounds show a high and selective binding affinity to the histamine H3 receptor indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity. As a result, the compounds are useful for the treatment of diseases and disorders related to the histamine H3 receptor.
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