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7-(benzyloxy)-6-d3-methoxyquinazolin-4(3H)-one | 1174397-22-8

中文名称
——
中文别名
——
英文名称
7-(benzyloxy)-6-d3-methoxyquinazolin-4(3H)-one
英文别名
7-phenylmethoxy-6-(trideuteriomethoxy)-3H-quinazolin-4-one
7-(benzyloxy)-6-d3-methoxyquinazolin-4(3H)-one化学式
CAS
1174397-22-8
化学式
C16H14N2O3
mdl
——
分子量
285.275
InChiKey
ZCUFFSHMOAEEIL-FIBGUPNXSA-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):
    2.1
  • 重原子数:
    21
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    59.9
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • VANDETANIB DERIVATIVES
    申请人:Tung Roger
    公开号:US20110117084A1
    公开(公告)日:2011-05-19
    This invention relates to novel quinazoline derivatives and their acceptable acid addition salts. The invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions beneficially treated by inhibitory activity against the VEGF receptor tyrosine kinase.
    本发明涉及新型喹噁啉衍生物及其可接受的酸盐。本发明还提供了包含本发明化合物的组合物,并且使用这种组合物治疗通过抑制VEGF受体酪氨酸激酶活性有益治疗的疾病和病症的方法。
  • US8609673B2
    申请人:——
    公开号:US8609673B2
    公开(公告)日:2013-12-17
  • [EN] QUINAZOLINE COMPOUNDS AND METHODS OF TREATING CANCER<br/>[FR] COMPOSÉS DE QUINAZOLINE ET MÉTHODES DE TRAITEMENT DU CANCER
    申请人:CONCERT PHARMACEUTICALS INC
    公开号:WO2009094211A1
    公开(公告)日:2009-07-30
    This invention relates to novel quinazolines, their derivatives, pharmaceutically acceptable salts, solvates, and hydrates thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering an inhibitor of angiogenesis and vascular endothelial growth factor receptor (VEGF) kinases.
  • [EN] VANDETANIB DERIVATIVES<br/>[FR] DÉRIVÉS DE VANDETANIB
    申请人:CONCERT PHARMACEUTICALS INC
    公开号:WO2009094210A1
    公开(公告)日:2009-07-30
    This invention relates to novel quinazoline derivatives and their acceptable acid addition salts. The invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions beneficially treated by inhibitory activity against the VEGF receptor tyrosine kinase.
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