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5-{2-(4-(4-ethylpiperazin-1-yl)phenyl)pyridin-4-yl}-4-(6-methyl-pyridin-2-yl)-1,3-thiazol-2-ylamine | 656257-90-8

中文名称
——
中文别名
——
英文名称
5-{2-(4-(4-ethylpiperazin-1-yl)phenyl)pyridin-4-yl}-4-(6-methyl-pyridin-2-yl)-1,3-thiazol-2-ylamine
英文别名
5-[2-[4-(4-Ethylpiperazin-1-yl)phenyl]pyridin-4-yl]-4-(6-methylpyridin-2-yl)-1,3-thiazol-2-amine
5-{2-(4-(4-ethylpiperazin-1-yl)phenyl)pyridin-4-yl}-4-(6-methyl-pyridin-2-yl)-1,3-thiazol-2-ylamine化学式
CAS
656257-90-8
化学式
C26H28N6S
mdl
——
分子量
456.615
InChiKey
FXAXTKVHVOPEFW-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:
    33
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    99.4
  • 氢给体数:
    1
  • 氢受体数:
    7

文献信息

  • Compounds
    申请人:Dodic Nerina
    公开号:US20060004051A1
    公开(公告)日:2006-01-05
    The invention relates to novel aminothiazole derivatives which are inhibitors of the transforming growth factor, (“TGF”)-β signalling pathway, in particular, the phosphorylation of smad2 or smad3 by the TGF-β type I or activin-like kinase (“ALK”)-5 receptor, methods for their preparation and their use in medicine, specifically in the treatment and prevention of a disease state mediated by this pathway.
    本发明涉及一种新型的氨基噻唑衍生物,该衍生物是转化生长因子(“TGF”)-β信号通路的抑制剂,特别是抑制TGF-β类型I或类激活素样激酶(“ALK”)-5受体对smad2或smad3的磷酸化,以及该衍生物的制备方法和在医学上的应用,具体地用于治疗和预防由该通路介导的疾病状态。
  • COMPOUNDS
    申请人:SMITHKLINE BEECHAM CORPORATION
    公开号:EP1554275A2
    公开(公告)日:2005-07-20
  • [EN] COMPOUNDS<br/>[FR] COMPOSES
    申请人:SMITHKLINE BEECHAM CORP
    公开号:WO2004013134A2
    公开(公告)日:2004-02-12
    The invention relates to novel aminothiazole derivatives which are inhibitors of the transforming growth factor, ('TGF')-ß signalling pathway, in particular, the phosphorylation of smad2 or smad3 by the TGF-β type I or activin-like kinase ('ALK')-5 receptor, methods for their preparation and their use in medicine, specifically in the treatment and prevention of a disease state mediated by this pathway.
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