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N-[[5-[3-(1H-benzimidazol-2-yl)-1H-indazol-5-yl]-4-chloropyridin-3-yl]methyl]ethanamine | 1331747-08-0

中文名称
——
中文别名
——
英文名称
N-[[5-[3-(1H-benzimidazol-2-yl)-1H-indazol-5-yl]-4-chloropyridin-3-yl]methyl]ethanamine
英文别名
——
N-[[5-[3-(1H-benzimidazol-2-yl)-1H-indazol-5-yl]-4-chloropyridin-3-yl]methyl]ethanamine化学式
CAS
1331747-08-0
化学式
C22H19ClN6
mdl
——
分子量
402.886
InChiKey
GCWOSFZYVIQUOG-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):
    3.7
  • 重原子数:
    29
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    82.3
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-3-carbaldehyde 在 potassium phosphate四(三苯基膦)钯sodium hydrogensulfite 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 26.0h, 生成 N-[[5-[3-(1H-benzimidazol-2-yl)-1H-indazol-5-yl]-4-chloropyridin-3-yl]methyl]ethanamine
    参考文献:
    名称:
    Discovery of indazoles as inhibitors of Tpl2 kinase
    摘要:
    Synthesis, modeling and structure-activity relationship of indazoles as inhibitors of Tpl2 kinase are described. From a high throughput screening effort, we identified an indazole hit compound 5 that has a single digit micromolar Tpl2 activity. Through SAR modifications at the C3 and C5 positions of the indazole, we discovered compound 31 with good potency in LANCE assay and cell-based p-Erk assay. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.06.065
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文献信息

  • 3-(BENZOIMIDAZOL-2-YL)-INDAZOLE INHIBITORS OF THE WNT SIGNALING PATHWAY AND THERAPEUTIC USES THEREOF
    申请人:Samumed, LLC
    公开号:US20140194441A1
    公开(公告)日:2014-07-10
    Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease, lung disease and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases and neurological conditions/disorders/diseases due to mutations or dysregulation of the Wnt pathway and/or of one or more of Wnt signaling components. Also provided are methods for treating Wnt-related disease states.
    揭示了用于治疗各种疾病和病理的吲唑化合物。更具体地,本公开涉及使用吲唑化合物或其类似物治疗由Wnt途径信号激活所特征的疾病(例如癌症、异常细胞增殖、血管生成、阿尔茨海默病、肺部疾病和骨关节炎),调节由Wnt途径信号介导的细胞事件,以及由于Wnt途径和/或一个或多个Wnt信号组分的突变或失调而导致的遗传疾病和神经系统疾病/疾患/疾病。还提供了治疗与Wnt相关疾病状态的方法。
  • 3-(benzoimidazol-2-yl)-indazole inhibitors of the Wnt signaling pathway and therapeutic uses thereof
    申请人:Samumed, LLC
    公开号:US10183929B2
    公开(公告)日:2019-01-22
    Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease, lung disease and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases and neurological conditions/disorders/diseases due to mutations or dysregulation of the Wnt pathway and/or of one or more of Wnt signaling components. Also provided are methods for treating Wnt-related disease states.
    本发明公开了用于治疗各种疾病和病理的吲唑化合物。更具体地说,本公开涉及吲唑化合物或其类似物在治疗以 Wnt 通路信号激活为特征的疾病(如癌症、异常细胞增殖、血管生成、阿尔茨海默病、肺病和骨关节炎)中的用途,以及吲唑化合物或其类似物的调节作用、癌症、异常细胞增殖、血管生成、阿尔茨海默病、肺病和骨关节炎)、Wnt 通路信号介导的细胞事件的调节,以及由于 Wnt 通路和/或一种或多种 Wnt 信号元件的突变或失调引起的遗传性疾病和神经系统状况/失调/疾病。此外,还提供了治疗 Wnt 相关疾病状态的方法。
  • 3-(benzoimidazol-2-YL)-indazole inhibitors of the Wnt signaling pathway and therapeutic uses thereof
    申请人:Samumed, LLC
    公开号:US10654832B2
    公开(公告)日:2020-05-19
    Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease, lung disease and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases and neurological conditions/disorders/diseases due to mutations or dysregulation of the Wnt pathway and/or of one or more of Wnt signaling components. Also provided are methods for treating Wnt-related disease states.
    本发明公开了用于治疗各种疾病和病理的吲唑化合物。更具体地说,本公开涉及吲唑化合物或其类似物在治疗以 Wnt 通路信号激活为特征的疾病(如癌症、异常细胞增殖、血管生成、阿尔茨海默病、肺病和骨关节炎)中的用途,以及吲唑化合物或其类似物的调节作用、癌症、异常细胞增殖、血管生成、阿尔茨海默病、肺病和骨关节炎)、Wnt 通路信号介导的细胞事件的调节,以及由于 Wnt 通路和/或一种或多种 Wnt 信号元件的突变或失调引起的遗传性疾病和神经系统状况/失调/疾病。此外,还提供了治疗 Wnt 相关疾病状态的方法。
  • US9908867B2
    申请人:——
    公开号:US9908867B2
    公开(公告)日:2018-03-06
  • [EN] 3-(BENZOIMIDAZOL-2-YL)-INDAZOLE INHIBITORS OF THE WNT SIGNALING PATHWAY AND THERAPEUTIC USES THEREOF<br/>[FR] INHIBITEURS DE 3-(BENZOIMIDAZOL-2-YL)-INDAZOLE DE LA VOIE DE SIGNALISATION PAR WNT ET LEURS UTILISATIONS THÉRAPEUTIQUES
    申请人:SAMUMED LLC
    公开号:WO2014110086A2
    公开(公告)日:2014-07-17
    Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease, lung disease and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases and neurological conditions/disorders/diseases due to mutations or dysregulation of the Wnt pathway and/or of one or more of Wnt signaling components. Also provided are methods for treating Wnt-related disease states.
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