4-{[6-(4-{[(4-fluorophenyl)-acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-methoxy-N-[2-(methylsulfonyl)ethyl]benzamide | 1403331-20-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 4-{[6-(4-{[(4-fluorophenyl)-acetyl]amino}phenyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino}-3-methoxy-N-[2-(methylsulfonyl)ethyl]benzamide
• 英文别名: 4-[[6-[4-[[2-(4-fluorophenyl)acetyl]amino]phenyl]-[1,2,4]triazolo[1,5-a]pyridin-2-yl]amino]-3-methoxy-N-(2-methylsulfonylethyl)benzamide
• CAS: 1403331-20-3
• 化学式: C₃₁H₂₉FN₆O₅S
• 分子量: 616.673
• InChiKey: NIGBOUJVBLXXPE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  44
• 可旋转键数：
  11
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  152
• 氢给体数：
  3
• 氢受体数：
  9

文献信息

• METHOD FOR PREPARING SUBSTITUTED TRIAZOLOPYRIDINES
  申请人：BAYER PHARMA AKTIENGESELLSCHAFT

  公开号：US20150148542A1

  公开（公告）日：2015-05-28

  The present invention relates to methods of preparing substituted triazolopyridine compounds of general formula (I) as described and defined herein, as well as to intermediate compounds useful in the preparation of said compounds.

  本发明涉及根据本文所描述和定义的一般式（I）制备取代三唑吡啶化合物的方法，以及用于制备所述化合物的中间体化合物。
• TRIAZOLOPYRIDINES
  申请人：Bayer Intellectual Property GmbH

  公开号：EP2699575B1

  公开（公告）日：2015-03-25
• US9388177B2
  申请人：——

  公开号：US9388177B2

  公开（公告）日：2016-07-12
• [EN] COMBINATIONS FOR THE TREATMENT OF CANCER<br/>[FR] COMBINAISONS POUR LE TRAITEMENT DU CANCER
  申请人：BAYER PHARMA AG

  公开号：WO2014020043A1

  公开（公告）日：2014-02-06

  The present invention relates to combinations of at least two compounds A and B, compound A being an inhibitor of Mps-1 kinase, and compound B being an inhibitor of an anti-apoptotic protein of the Bcl-2 family. Another aspect of the present invention relates to the use of such combinations as described supra for the preparation of a medicament for the treatment or prophylaxis of a disease, particurlarly for the treatment of cancer. Another aspect of the present invention relates to the use of an anti-apoptotic protein from the Bcl-2 family as a sensitizer of cells to Mps-1 inhibitors. Another aspect of the present invention relates to the use of the ratio of pro-apoptotic and anti-apoptotic proteins from the Bcl-2 family in a biological sample as a biomarker for a Mps-1 kinase inhibitor treatment.