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Piperazine,1-[(7-cyano-4-methoxy-1h-indol-3-yl)oxoacetyl]-4-(1-isoquinolinyl)-

中文名称
——
中文别名
——
英文名称
Piperazine,1-[(7-cyano-4-methoxy-1h-indol-3-yl)oxoacetyl]-4-(1-isoquinolinyl)-
英文别名
3-[2-(4-isoquinolin-1-ylpiperazin-1-yl)-2-oxoacetyl]-4-methoxy-1H-indole-7-carbonitrile
Piperazine,1-[(7-cyano-4-methoxy-1h-indol-3-yl)oxoacetyl]-4-(1-isoquinolinyl)-化学式
CAS
——
化学式
C25H21N5O3
mdl
——
分子量
439.5
InChiKey
WXMQQTYWWGPWHP-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):
    3.2
  • 重原子数:
    33
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    102
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • INDOLE, AZAINDOLE AND RELATED HETEROCYCLIC N-SUBSTITUTED PIPERAZINE DERIVATIVES
    申请人:Yeung Kap-Sun
    公开号:US20080132516A1
    公开(公告)日:2008-06-05
    This invention provides compounds of Formula I, including pharmaceutically acceptable salts thereof, having drug and bio-affecting properties, their pharmaceutical compositions and method of use. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS. The compounds of Formula I have the formula wherein: Z is Q is selected from the group consisting of m is 2; A is selected from the group consisting of cinnolinyl, napthyridinyl, quinoxalinyl, pyridinyl, pyrimidinyl, quinolinyl, isoquinolinyl, quinazolinyl, azabenzofuryl, and phthalazinyl each of which may be optionally substituted with one or two groups independently selected from methyl, methoxy, hydroxy, amino and halogen; and —W— is
  • US8039486B2
    申请人:——
    公开号:US8039486B2
    公开(公告)日:2011-10-18
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