5-phenyl-(1H-pyrrolo[2,3-b]pyridine-5-yl)-amine | 858116-85-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并吡啶类
• 英文名称: 5-phenyl-(1H-pyrrolo[2,3-b]pyridine-5-yl)-amine
• 英文别名: phenyl-(1H-pyrrolo[2,3-b]pyridin-5-yl)-amine；phenyl-(1H-pyrrolo[2,3-b]pyridine-5-yl)-amine；N-phenyl-1H-pyrrolo[2,3-b]pyridin-5-amine
• CAS: 858116-85-5
• 化学式: C₁₃H₁₁N₃
• 分子量: 209.25
• InChiKey: BWWVHFFBJATQFG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  40.7
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  5-phenyl-(1H-pyrrolo[2,3-b]pyridine-5-yl)-amine 、 N-(2,4-二氟-3-甲酰基苯基)-1-丙烷磺酰胺 在 氢氧化钾 作用下， 以 甲醇 为溶剂， 反应 12.0h， 以50%的产率得到propane-1-sulfonic acid {2,4-difluoro-3-[hydroxy-(5-phenylamino-1H-pyrrolo[2,3-b]pyridin-3-yl)-methyl]-phenyl}-amide
  参考文献：
  名称：

  WO2007/2325

  摘要：

  公开号：
• 作为产物：
  描述：

  5-phenyl-(1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine-5-yl)-amine 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 反应 1.0h， 以76%的产率得到5-phenyl-(1H-pyrrolo[2,3-b]pyridine-5-yl)-amine
  参考文献：
  名称：

  COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR

  摘要：

  描述了对蛋白激酶活性有作用的化合物，以及使用这些化合物来治疗与蛋白激酶异常活性相关的疾病和病况的方法。

  公开号：

  US20080167338A1

文献信息

• Novel Compounds for the Treatment of Diseases Associated with Amyloid or Amyloid-Like Proteins
  申请人：Kroth Heiko

  公开号：US20110280808A1

  公开（公告）日：2011-11-17

  The present invention relates to novel compounds that can be employed in the treatment of a group of disorders and abnormalities associated with amyloid protein, such as Alzheimer's disease, and of diseases or conditions associated with amyloid-like proteins. The compounds of the present invention can also be used in the treatment of ocular diseases associated with pathological abnormalities/changes in the tissues of the visual system. The present invention further relates to pharmaceutical compositions comprising these compounds and to the use of these compounds for the preparation of medicaments for treating or preventing diseases or conditions associated with amyloid and/or amyloid-like proteins. A method of treating or preventing diseases or conditions associated with amyloid and/or amyloid-like proteins is also disclosed.

  本发明涉及一种新型化合物，可用于治疗与淀粉样蛋白相关的一组疾病和异常，如阿尔茨海默病，以及与淀粉样蛋白类似蛋白相关的疾病或病况。本发明的化合物还可用于治疗与视觉系统组织中的病理异常/变化相关的眼部疾病。本发明还涉及包含这些化合物的药物组合物，以及利用这些化合物制备用于治疗或预防与淀粉样和/或淀粉样类似蛋白相关的疾病或病况的药物的用途。还公开了一种治疗或预防与淀粉样和/或淀粉样类似蛋白相关的疾病或病况的方法。
• Compounds and methods for development of Ret modulators
  申请人：Ibrahim Prabha

  公开号：US20070049615A1

  公开（公告）日：2007-03-01

  Compounds active on Ret are described, as well as methods of using such compounds. Also described are crystal structures of Ret surrogates that were determined using X-ray crystallography. The use of such Ret surrogate crystals and strucural information can, for example, be used for identifying molecular scaffolds and for developing ligands that bind to and modulate Ret and for identifying improved ligands based on known ligands.

  描述了对Ret具有活性的化合物，以及使用这些化合物的方法。还描述了通过X射线晶体学确定的Ret替代物的晶体结构。例如，使用这些Ret替代物晶体和结构信息可以用于识别分子支架，开发与Ret结合并调节其活性的配体，以及基于已知配体识别改进的配体。
• NEW IMIDAZOLONE DERIVATIVES, PREPARATION THEREOF AS DRUGS, PHARMACEUTICAL COMPOSITIONS, AND USE THEREOF AS PROTEIN KINASE INHIBITORS, IN PARTICULAR CDC7
  申请人：Leroy Vincent

  公开号：US20090253679A1

  公开（公告）日：2009-10-08

  The present invention relates to imidazolone derivatives of formula (I) to methods of preparing such derivatives, intermediates thereto, pharmaceutical compositions comprising such derivatives, and methods of inhibiting protein kinase, and methods of treatment comprising administration of such derivatives.

  本发明涉及式(I)的咪唑酮衍生物，涉及制备这种衍生物的方法、中间体、包含这种衍生物的药物组合物、抑制蛋白激酶的方法以及包括给予这种衍生物的治疗方法。
• PYRROLO[2,3-B]PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS
  申请人：PLEXXIKON INC.

  公开号：EP3088400A1

  公开（公告）日：2016-11-02

  Compounds active on protein kinases are described, as well as methods of using such compounds to treat diseases and conditions associated with aberrant activity of protein kinases.

  本文描述了对蛋白激酶活性产生作用的化合物，以及使用这些化合物治疗与蛋白激酶异常活性相关的疾病和病况的方法。
• Compounds and methods for development of RET modulators
  申请人：Ibrahim Prabha

  公开号：US20070066641A1

  公开（公告）日：2007-03-22

  Compounds active on Ret and/or FGFR are described, as well as methods of using such compounds. Also described are crystal structures of Ret surrogates that were determined using X-ray crystallography. The use of such Ret surrogate crystals and structural information can, for example, be used for identifying molecular scaffolds and for developing ligands that bind to and modulate Ret and for identifying improved ligands based on known ligands.

  本文描述了在Ret和/或FGFR上活性化合物，以及使用这些化合物的方法。还描述了使用X射线晶体学确定的Ret代用品的晶体结构。例如，可以利用这些Ret代用品晶体和结构信息来识别分子支架并开发结合和调节Ret的配体，以及基于已知配体识别改进的配体。