7-Ethenylpyrrolo[2,1-f][1,2,4]triazin-4-amine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并三嗪类
• 英文名称: 7-Ethenylpyrrolo[2,1-f][1,2,4]triazin-4-amine
• 英文别名: 7-ethenylpyrrolo[2,1-f][1,2,4]triazin-4-amine
• 化学式: C₈H₈N₄
• 分子量: 160.18
• InChiKey: LLSQLNHWCVHBOY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  56.2
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• PYRROLOTRIAZINE COMPOUNDS AS TAM INHIBITORS
  申请人：Incyte Corporation

  公开号：US20170275290A1

  公开（公告）日：2017-09-28

  This application relates to compounds of Formula I: or pharmaceutically acceptable salts thereof, which are inhibitors of TAM kinases which are useful for the treatment of disorders such as cancer.

  这个应用涉及到Formula I的化合物： 或其药用可接受的盐，这些化合物是TAM激酶的抑制剂，可用于治疗癌症等疾病。
• TYROSINE KINASE INHIBITORS
  申请人：Principia Biopharma Inc.

  公开号：US20140309223A1

  公开（公告）日：2014-10-16

  The present disclosure provides compounds and pharmaceutically acceptable salts thereof that are tyrosine kinase inhibitors, in particular BLK, BMX, EGFR, HER2, HER4, ITK, TEC, BTK, and TXK and are therefore useful for the treatment of diseases treatable by inhibition of tyrosine kinases such as cancer and inflammatory diseases such as arthritis, and the like. Also provided are pharmaceutical compositions containing such compounds and pharmaceutically acceptable salts thereof and processes for preparing such compounds and pharmaceutically acceptable salts thereof.

  本公开提供化合物及其药学上可接受的盐，它们是酪氨酸激酶抑制剂，特别是BLK、BMX、EGFR、HER2、HER4、ITK、TEC、BTK和TXK，因此可用于治疗通过抑制酪氨酸激酶治疗的疾病，如癌症和炎症性疾病，如关节炎等。还提供了含有这些化合物及其药学上可接受的盐的药物组合物和制备这些化合物及其药学上可接受的盐的方法。
• SUBSTITUTED BENZOTHIENYL-PYRROLOTRIAZINES AND USES THEREOF
  申请人：Bayer Intellectual Property GmbH

  公开号：US20150031676A1

  公开（公告）日：2015-01-29

  This invention relates to novel substituted 5-(1-benzothiophen-2-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine derivatives having protein tyrosine kinase inhibitory activities, to processes for the preparation of such compounds, to pharmaceutical compositions containing such compounds, and to the use of such compounds or compositions for treating proliferative disorders, in particular cancer and tumor diseases.

  本发明涉及一种新型取代的5-(1-苯并噻吩-2-基)吡咯并[2,1-f][1,2,4]三嗪-4-胺衍生物，具有蛋白酪氨酸激酶抑制活性，以及制备这种化合物的过程，含有这种化合物的制药组合物，以及使用这种化合物或组合物治疗增生性疾病，特别是癌症和肿瘤疾病。
• Pyrrolotriazine compounds as TAM inhibitors
  申请人：Incyte Corporation

  公开号：US10442810B2

  公开（公告）日：2019-10-15

  This application relates to compounds of Formula I: or pharmaceutically acceptable salts thereof, which are inhibitors of TAM kinases which are useful for the treatment of disorders such as cancer.

  本申请涉及式 I 的化合物： 或其药学上可接受的盐类，它们是 TAM 激酶的抑制剂，可用于治疗癌症等疾病。
• US8759358B1
  申请人：——

  公开号：US8759358B1

  公开（公告）日：2014-06-24