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4-(1-benzyl-piperidin-4-yl)-1-(5-isopropyl-2,4-bismethoxymethoxy-benzoyl) thiosemicarbazide | 909871-35-8

中文名称
——
中文别名
——
英文名称
4-(1-benzyl-piperidin-4-yl)-1-(5-isopropyl-2,4-bismethoxymethoxy-benzoyl) thiosemicarbazide
英文别名
1-(1-benzylpiperidin-4-yl)-3-[[2,4-bis(methoxymethoxy)-5-propan-2-ylbenzoyl]amino]thiourea
4-(1-benzyl-piperidin-4-yl)-1-(5-isopropyl-2,4-bismethoxymethoxy-benzoyl) thiosemicarbazide化学式
CAS
909871-35-8
化学式
C27H38N4O5S
mdl
——
分子量
530.689
InChiKey
WRINWOVEVMLTDH-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):
    4.2
  • 重原子数:
    37
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    125
  • 氢给体数:
    3
  • 氢受体数:
    7

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

点击查看最新优质反应信息

文献信息

  • Novel Hsp90 Inhibitor
    申请人:Kuramochi Hiroshi
    公开号:US20080269218A1
    公开(公告)日:2008-10-30
    Disclosed is a triazole derivative represented by the general formula (1) below or a pharmacologically acceptable salt thereof. Also disclosed are a prodrug of such a triazole derivative and an HSP90 inhibitor containing any one of them as an active constituent. (1) (In the formula, X represents a halogen atom, an optionally substituted alkyl group, an optionally substituted alkenyl group or the like; Y represents a mercapto group, a hydroxyl group, an optionally substituted sulfonyl group, an optionally substituted amino group or the like; and R represents an optionally substituted aryl or amino group or the like.)
    本发明公开了一种由下述通式(1)表示的三唑衍生物或其药物可接受的盐。还公开了这种三唑衍生物的前药和含有其中任何一种作为活性成分的HSP90抑制剂。(1) (在公式中,X代表卤素原子,可选取代的烷基,可选取代的烯基或类似物; Y代表巯基,羟基,可选取代的磺酰基,可选取代的氨基或类似物; R代表可选取代的芳基或氨基或类似物。)
  • HSP90 inhibitor
    申请人:Kuramochi Hiroshi
    公开号:US08399464B2
    公开(公告)日:2013-03-19
    Disclosed is a triazole derivative(s) represented by the general formula (1) below or a pharmacologically acceptable salt(s) thereof. Also disclosed are a prodrug(s) of such a triazole derivative(s) and an HSP90 inhibitor(s) containing any one of them as an active constituent. (1) (In the formula, X represents a halogen atom, an optionally substituted alkyl group, an optionally substituted alkynyl group or the like; Y represents a mercapto group, a hydroxyl group, an optionally substituted sulfonyl group, an optionally substituted amino group or the like; and R represents an optionally substituted aryl or alkyl group or the like.)
    本发明公开了一种由下式(1)表示的三唑衍生物或其药理学上可接受的盐。还公开了这种三唑衍生物的前药以及含有其中任何一种作为活性成分的HSP90抑制剂。(1)(在该式中,X代表卤素原子,可选取代的烷基,可选取代的炔基或类似物;Y代表巯基,羟基,可选取代的磺酰基,可选取代的氨基或类似物;R代表可选取代的芳基或烷基或类似物。)
  • Novel HSP90 Inhibitor
    申请人:NIPPON KAYAKU KABUSHIKI KAISHA
    公开号:US20130116252A1
    公开(公告)日:2013-05-09
    Disclosed is a triazole derivative(s) represented by the general formula (1) below or a pharmacologically acceptable salt(s) thereof. Also disclosed are a prodrug(s) of such a triazole derivative(s) and an HSP90 inhibitor(s) containing any one of them as an active constituent. (1) (In the formula, X represents a halogen atom, an optionally substituted alkyl group, an optionally substituted alkynyl group or the like; Y represents a mercapto group, a hydroxyl group, an optionally substituted sulfonyl group, an optionally substituted amino group or the like; and R represents an optionally substituted aryl or alkyl group or the like.)
    本发明涉及一种由下式(1)表示的三唑衍生物或其药理学上可接受的盐。本发明还涉及此类三唑衍生物的前药以及含有其中任何一种作为活性成分的HSP90抑制剂。式中,X代表卤素原子,可选取代的烷基,可选取代的炔基或类似物;Y代表巯基,羟基,可选取代的磺酰基,可选取代的氨基或类似物;R代表可选取代的芳基或烷基或类似物。
  • NOVEL HSP90 INHIBITOR
    申请人:NIPPON KAYAKU KABUSHIKI KAISHA
    公开号:EP1857446A1
    公开(公告)日:2007-11-21
    Disclosed is a triazole derivative represented by the general formula (1) below or a pharmacologically acceptable salt thereof. Also disclosed are a prodrug of such a triazole derivative and an HSP90 inhibitor containing any one of them as an active constituent. (1) (In the formula, X represents a halogen atom, an optionally substituted alkyl group, an optionally substituted alkenyl group or the like; Y represents a mercapto group, a hydroxyl group, an optionally substituted sulfonyl group, an optionally substituted amino group or the like; and R represents an optionally substituted aryl or amino group or the like.)
    本发明公开了如下通式(1)所代表的三唑衍生物或其药理学上可接受的盐。还公开了这种三唑衍生物的原药和含有其中任一种作为活性成分的 HSP90 抑制剂。(1)(式中,X代表卤原子、任选取代的烷基、任选取代的烯基或类似物;Y代表巯基、羟基、任选取代的磺酰基、任选取代的氨基或类似物;R代表任选取代的芳基或氨基或类似物)。
  • US8399464B2
    申请人:——
    公开号:US8399464B2
    公开(公告)日:2013-03-19
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