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2-(1H-indazol-3-yl)-3H-imidazo[4,5-c]pyridine | 485834-70-6

中文名称
——
中文别名
——
英文名称
2-(1H-indazol-3-yl)-3H-imidazo[4,5-c]pyridine
英文别名
——
2-(1H-indazol-3-yl)-3H-imidazo[4,5-c]pyridine化学式
CAS
485834-70-6
化学式
C13H9N5
mdl
MFCD19126760
分子量
235.248
InChiKey
DQAXLZZLXDDPJG-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):
    1.7
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    70.2
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • 2-(1H-INDAZOL-3-YL)-1H-IMIDAZO[4,5-C]PYRIDINE AND THERAPEUTIC USES THEREOF
    申请人:Samumed, LLC
    公开号:US20160075701A1
    公开(公告)日:2016-03-17
    Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present invention 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, fibrotic disorders, bone or cartilage diseases, 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.
    披露了用于治疗各种疾病和病理的吲唑化合物。更具体地,本发明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、纤维化疾病、骨骼或软骨疾病和骨关节炎),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病症/疾病。还提供了治疗与Wnt相关疾病状态的方法。
  • Benzimidazoles
    申请人:Edwards L. Michael
    公开号:US20060014756A1
    公开(公告)日:2006-01-19
    The invention is directed to physiologically active compounds of the general formula (Ix) and compositions containing such compounds, and their prodrugs, and pharmaceutically acceptable salts and solvates of such compounds and their prodrugs, as well as to novel compounds within the scope of formula (Ix), and to processes for their preparation. Such compounds and compositions have valuable pharmaceutical properties, in particular the ability to inhibit kinases.
    本发明涉及一般式(Ix)的生理活性化合物及含有这种化合物的组合物,以及它们的前药、药学上可接受的盐和溶剂化物,还涉及在式(Ix)范围内的新化合物和它们的制备方法。这种化合物和组合物具有有价值的药物性质,特别是抑制激酶的能力。
  • Indazole benzimidazole compounds
    申请人:Jansen M. Johanna
    公开号:US20060079564A1
    公开(公告)日:2006-04-13
    Organic compounds having the structure I are provided where the variables have the values described herein. A method of inhibiting c-ABL in a patient includes administering an effective amount of a compound of structure I, a tautomer of the compound, a pharmaceutically acceptable salt of the compound, or a pharmaceutically acceptable salt of the tautomer to the patient.
    提供具有结构I的有机化合物,其中变量具有所述值。一种抑制患者中c-ABL的方法包括向患者投与结构I的化合物,化合物的互变异构体,化合物的药学上可接受的盐或互变异构体的药学上可接受的盐的有效量。
  • 2-(1H-indazol-3-yl)-1H-imidazo[4,5-C]pyridine and therapeutic uses thereof
    申请人:Samumed, LLC
    公开号:US10081631B2
    公开(公告)日:2018-09-25
    Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present invention 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, fibrotic disorders, bone or cartilage diseases, 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,本发明涉及一种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、纤维化疾病、骨或软骨疾病以及骨关节炎)中的用途、癌症、异常细胞增殖、血管生成、纤维化疾病、骨或软骨疾病和骨关节炎)、调节由 Wnt 通路信号介导的细胞事件,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疾病和神经系统疾病/失调/疾病。此外,还提供了治疗 Wnt 相关疾病状态的方法。
  • BENZIMIDAZOLES AND ANALOGUES AND THEIR USE AS PROTEIN KINASES INHIBITORS
    申请人:Aventis Pharmaceuticals Inc.
    公开号:EP1441725A1
    公开(公告)日:2004-08-04
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