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N-[[5-[3-(1H-benzimidazol-2-yl)-1H-indazol-5-yl]-4-methylpyridin-3-yl]methyl]ethanamine | 351456-23-0

中文名称
——
中文别名
——
英文名称
N-[[5-[3-(1H-benzimidazol-2-yl)-1H-indazol-5-yl]-4-methylpyridin-3-yl]methyl]ethanamine
英文别名
——
N-[[5-[3-(1H-benzimidazol-2-yl)-1H-indazol-5-yl]-4-methylpyridin-3-yl]methyl]ethanamine化学式
CAS
351456-23-0
化学式
C23H22N6
mdl
——
分子量
382.468
InChiKey
AWWXCJOYTYVQJQ-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):
    3.5
  • 重原子数:
    29
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.17
  • 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-methylpyridin-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。
  • INDAZOLES AS WNT/B-CATENIN SIGNALING PATHWAY INHIBITORS AND THERAPEUTIC USES THEREOF
    申请人:Hood John
    公开号:US20110034441A1
    公开(公告)日:2011-02-10
    Described herein are methods of treating a disorder or disease in which aberrant Wnt signaling is implicated, with a variety of compounds, including Wnt inhibitor compounds. More particularly, it 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 and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases due to mutations in Wnt signaling components.
    本文描述了一种治疗与异常Wnt信号传导有关的疾病或紊乱的方法,使用各种化合物,包括Wnt抑制剂化合物。更具体地,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(如癌症、异常细胞增殖、血管生成、阿尔茨海默病和骨关节炎),调节由Wnt途径信号介导的细胞事件,以及由于Wnt信号传导组分突变引起的遗传疾病。
  • Indazole compounds, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation
    申请人:Reich Heinz Siegfried
    公开号:US20050239855A1
    公开(公告)日:2005-10-27
    Indazole compounds that modulate and/or inhibit cell proliferation, such as the activity of protein kinases are described. These compounds and pharmaceutical compositions containing them are capable of mediating, e.g., kinases-dependent diseases to modulate and/or inhibit unwanted cell proliferation. The invention is also directed to the therapeutic or prophylactic use of pharmaceutical compositions containing such compounds, and to methods of treating cancer as well as other disease states associated with unwanted angiogenesis and/or cellular proliferation, such as diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, and psoriasis, by administering effective amounts of such compounds.
    本文描述了调节和/或抑制细胞增殖的吲唑化合物,例如蛋白激酶的活性。这些化合物和含有它们的药物组合物能够介导依赖于激酶的疾病,以调节和/或抑制不想要的细胞增殖。本发明还涉及含有这些化合物的药物组合物的治疗或预防用途,以及通过给予有效量的这些化合物治疗癌症以及其他与不想要的血管生成和/或细胞增殖相关的疾病状态,如糖尿病性视网膜病变、新生血管性青光眼、类风湿性关节炎和牛皮癣的方法。
  • 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。
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