5-吡啶-3-基-1H-吲唑 | 885272-37-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡唑类
• 中文名称: 5-吡啶-3-基-1H-吲唑
• 英文名称: 5-pyridin-3-ylindazole
• 英文别名: algernon；Compound No.688；5-Pyridin-3-YL-1H-indazole
• CAS: 885272-37-7
• 化学式: C₁₂H₉N₃
• mdl: MFCD04114676
• 分子量: 195.224
• InChiKey: RXWLUAHKORPFPY-UHFFFAOYSA-N

物化性质

• 沸点：
  434.9±20.0 °C(Predicted)
• 密度：
  1.270±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  41.6
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 海关编码：
  2933990090

反应信息

• 作为产物：
  描述：

  5-pyridin-3-yl-indazole-1-carboxylic acid tert-butyl ester 在 3-甲氧基丙胺 作用下， 以 四氢呋喃 为溶剂， 以48%的产率得到5-吡啶-3-基-1H-吲唑
  参考文献：
  名称：

  通过3-甲氧基丙胺加成-消除对N-叔丁氧羰基（Boc）保护的官能化杂芳烃的脱保护

  摘要：

  描述了通过建议的添加/消除机理将3-甲氧基丙胺用作各种N- Boc保护的杂芳烃的温和脱保护剂。本文报道了方法开发，对各种杂芳烃的应用，包括吲哚，1,2-吲唑，1,2-吡唑和相关衍生物，十倍放大反应以及初步机理假设的实验评估。

  DOI：

  10.1002/ejoc.201901811

文献信息

• Indazole compounds, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation
  申请人：——

  公开号：US20020161022A1

  公开（公告）日：2002-10-31

  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.

  描述了调节和/或抑制细胞增殖的吲唑化合物，例如蛋白激酶活性。这些化合物和含有它们的药物组合物能够介导，例如，依赖激酶的疾病，以调节和/或抑制不需要的细胞增殖。该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，以及通过给予这些化合物的有效量来治疗癌症以及与不需要的血管生成和/或细胞增殖相关的其他疾病状态，如糖尿病视网膜病变、新生血管性青光眼、类风湿性关节炎和牛皮癣的方法。
• [EN] KINASE INHIBITOR COMPOUNDS AND COMPOSITIONS AND METHODS OF USE<br/>[FR] COMPOSÉS INHIBITEURS DE KINASE, COMPOSITIONS ET MÉTHODES D'UTILISATION
  申请人：ICAHN SCHOOL MED MOUNT SINAI

  公开号：WO2021263129A1

  公开（公告）日：2021-12-30

  Disclosed herein are kinase inhibitor compounds having the structure (I) or a stereoisomer, pharmaceutically acceptable salt, oxide, or solvate thereof, where R1, R2, X, L, Q, and Y are as defined herein. Also disclosed are compositions containing the kinase inhibitor compounds, methods of inhibiting activity of a kinase in a cell, methods of increasing cell proliferation in a population of pancreatic beta cells, methods of treating a subject for a condition associated with insufficient insulin secretion, and methods of treating a subject for a neurological disorder.

  本文披露了具有结构（I）或其立体异构体、药学上可接受的盐、氧化物或溶剂的激酶抑制剂化合物，其中R1、R2、X、L、Q和Y如本文所定义。还披露了含有激酶抑制剂化合物的组合物，抑制细胞中激酶活性的方法，增加胰岛β细胞群体中细胞增殖的方法，治疗因胰岛素分泌不足引起的疾病的方法，以及治疗神经系统疾病的方法。
• Cinnoline derivatives as phosphodiesterase 10 inhibitors
  申请人：Hitchcock A. Stephen

  公开号：US20070265270A1

  公开（公告）日：2007-11-15

  The present invention is directed to certain cinnoline compounds that are PDE10 inhibitors, pharmaceutical compositions containing such compounds and process for preparing such compounds. The invention is also directed to methods of treating diseases treatable by modulation of PDE10 enzyme, such as obesity, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.

  本发明涉及某些香豆素化合物，它们是PDE10抑制剂，包含这些化合物的制药组合物以及制备这些化合物的方法。本发明还涉及治疗可通过调节PDE10酶治疗的疾病的方法，如肥胖症、非胰岛素依赖性糖尿病、精神分裂症、双相障碍、强迫症等。
• Indazole compounds
  申请人：Ericsson M. Anna

  公开号：US20070282101A1

  公开（公告）日：2007-12-06

  Novel compounds of Formula (I) or pharmaceutically acceptable salts, prodrugs and biologically active metabolites thereof of Formula (I) wherein the substituents are as defined herein, which are useful as therapeutic agents.

  本发明提供了化合物(I)或其药学上可接受的盐、前药和生物活性代谢物，其中取代基如定义所述，这些化合物可用作治疗剂。
• Indazole Compounds
  申请人：Ericson Anna M.

  公开号：US20120053345A1

  公开（公告）日：2012-03-01

  Novel compounds of Formula (I) or pharmaceutically acceptable salts, prodrugs and biologically active metabolites thereof of Formula (I) wherein the substituents are as defined herein, which are useful as therapeutic agents.

  本发明涉及化合物(I)或其药学上可接受的盐、前药和生物活性代谢物，其中取代基的定义如本文所述，这些化合物可用作治疗剂。