N-(6-(1H-indol-4-yl)-1H-indazol-4-yl)-2-(piperidin-1-ylmethyl)thiazole-4-carboxamide | 1198433-43-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡唑类
• 英文名称: N-(6-(1H-indol-4-yl)-1H-indazol-4-yl)-2-(piperidin-1-ylmethyl)thiazole-4-carboxamide
• 英文别名: N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-2-(1-piperidinylmethyl)-1,3-thiazole-4-carboxamide；N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-2-(piperidin-1-ylmethyl)-1,3-thiazole-4-carboxamide
• CAS: 1198433-43-0
• 化学式: C₂₅H₂₄N₆OS
• 分子量: 456.571
• InChiKey: WPOHOQYMYXGMIB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  33
• 可旋转键数：
  5
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  118
• 氢给体数：
  3
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazol-4-amine 在 N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 、 sodium hydroxide 作用下， 以 水 、 N,N-二甲基甲酰胺 、 异丙醇 为溶剂， 反应 0.08h， 生成 N-(6-(1H-indol-4-yl)-1H-indazol-4-yl)-2-(piperidin-1-ylmethyl)thiazole-4-carboxamide
  参考文献：
  名称：

  Optimization of Novel Indazoles as Highly Potent and Selective Inhibitors of Phosphoinositide 3-Kinase δ for the Treatment of Respiratory Disease

  摘要：

  Optimization of lead compound 1, through extensive use of structure-based design and a focus on PI3K delta potency, isoform selectivity, and inhaled PK properties, led to the discovery of clinical candidates 2 (GSK2269557) and 3 (G5K2292767) for the treatment of respiratory indications via inhalation. Compounds 2 and 3 are both highly selective for PI3K delta over the closely related isoforms and are active in a disease relevant brown Norway rat acute OVA model of Th2-driven lung inflammation.

  DOI：

  10.1021/acs.jmedchem.5b00767

文献信息

• [EN] BENZPYRAZOL DERIVATIVES AS INHIBITORS OF PI3 KINASES<br/>[FR] DÉRIVÉS DE BENZPYRAZOLE EN TANT QU'INHIBITEURS DE P13 KINASES
  申请人：GLAXO GROUP LTD

  公开号：WO2009147188A1

  公开（公告）日：2009-12-10

  The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.

  这项发明涉及某些新颖化合物。具体来说，该发明涉及式(I)的化合物及其盐。该发明的化合物是PI3-激酶活性的抑制剂。
• BENZPYRAZOL DERIVATIVES AS INHIBITORS OF PI3 KINASES
  申请人：Baldwin Ian Robert

  公开号：US20110178063A1

  公开（公告）日：2011-07-21

  The invention is directed to certain novel compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.

  该发明涉及公式（I）的某些新化合物及其盐。该发明的化合物是PI3-激酶活性的抑制剂。
• Novel Use
  申请人：Baldwin Ian Robert

  公开号：US20130165433A1

  公开（公告）日：2013-06-27

  The present invention is directed to compounds for use in the treatment or prevention of influenza virus infection.

  本发明涉及用于治疗或预防流感病毒感染的化合物。
• US8658635B2
  申请人：——

  公开号：US8658635B2

  公开（公告）日：2014-02-25
• US9326987B2
  申请人：——

  公开号：US9326987B2

  公开（公告）日：2016-05-03