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2-[2-(3-ethyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino)-5-cyano-pyrimidin-4-ylamino]-N-methyl-benzamide | 1022964-28-8

中文名称
——
中文别名
——
英文名称
2-[2-(3-ethyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino)-5-cyano-pyrimidin-4-ylamino]-N-methyl-benzamide
英文别名
2-[[5-cyano-2-[(3-ethyl-1,2,4,5-tetrahydro-3-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]-N-methylbenzamide
2-[2-(3-ethyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino)-5-cyano-pyrimidin-4-ylamino]-N-methyl-benzamide化学式
CAS
1022964-28-8
化学式
C25H27N7O
mdl
——
分子量
441.536
InChiKey
AGNHISSLWAGXCY-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    33
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    106
  • 氢给体数:
    3
  • 氢受体数:
    7

文献信息

  • FUSED BICYCLIC DERIVATIVES OF 2,4-DIAMINOPYRIMIDINE AS ALK AND c-MET INHIBITORS
    申请人:Ahmed Gulzar
    公开号:US20090221555A1
    公开(公告)日:2009-09-03
    The present invention provides a compound of formula I or II or a pharmaceutically acceptable salt form thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , A 1 , A 2 , A 3 , A 4 , and A 5 , are as defined herein. The compounds of formula I or II have ALK and/or c-Met inhibitory activity, and may be used to treat proliferative disorders.
    本发明提供公式I或II化合物或其药学上可接受的盐形式,其中R1、R2、R3、R4、R5、A1、A2、A3、A4和A5如本文所定义。公式I或II化合物具有ALK和/或c-Met抑制活性,可用于治疗增殖性疾病。
  • Fused Bicyclic Derivatives of 2,4-Diaminopyrimidine as ALK and c-MET Inhibitors
    申请人:Ahmed Gulzar
    公开号:US20120165519A1
    公开(公告)日:2012-06-28
    The present invention provides a compound of formula I or II or a pharmaceutically acceptable salt form thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , A 1 , A 2 , A 3 , A 4 , and A 5 , are as defined herein. The compounds of formula I or II have ALK and/or c-Met inhibitory activity, and may be used to treat proliferative disorders.
    本发明提供了式I或II的化合物或其药学上可接受的盐形式,其中R1、R2、R3、R4、R5、A1、A2、A3、A4和A5如本文所定义。式I或II的化合物具有ALK和/或c-Met抑制活性,并可用于治疗增生性疾病。
  • PURINONE DERIVATIVES AS HM74A AGONISTS
    申请人:Incyte Corporation
    公开号:US20140371216A1
    公开(公告)日:2014-12-18
    The present invention relates to purinone derivatives which are agonists of the HM74a receptor. Further provided are compositions and methods of using the compounds herein, and their pharmaceutically acceptable salts for the treatment of disease.
    本发明涉及嘌呤酮衍生物,它们是HM74a受体激动剂。此外,还提供了使用本发明化合物及其药学上可接受的盐的组合物和方法,用于治疗疾病。
  • FUSED BICYCLIC DERIVATIVES OF 2,4-DIAMINOPYRIMIDINE AS ALK AND C-MET INHIBITORS
    申请人:Cephalon, Inc.
    公开号:EP2222647A1
    公开(公告)日:2010-09-01
  • Fused bicyclic derivatives of 2,4-diaminopyrimidine as alk and C-met inhibitors
    申请人:Cephalon, Inc.
    公开号:EP2684874B1
    公开(公告)日:2017-05-17
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