摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-fluoro-4-imidazo[4,5-c]pyridin-3-ylaniline | 774218-69-8

中文名称
——
中文别名
——
英文名称
2-fluoro-4-imidazo[4,5-c]pyridin-3-ylaniline
英文别名
——
2-fluoro-4-imidazo[4,5-c]pyridin-3-ylaniline化学式
CAS
774218-69-8
化学式
C12H9FN4
mdl
——
分子量
228.229
InChiKey
OZSQVSBUIYZRBY-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):
    2.14
  • 重原子数:
    17.0
  • 可旋转键数:
    1.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    56.73
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    2-fluoro-4-imidazo[4,5-c]pyridin-3-ylaniline吡啶盐酸甲醇4-二甲氨基吡啶 作用下, 以 二氯甲烷 为溶剂, 生成 1-(3-carbamimidoylphenyl)-N-(2-fluoro-4-{3H-imidazo[4,5-c]pyridin-3-yl}phenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide
    参考文献:
    名称:
    SAR and factor IXa crystal structure of a dual inhibitor of factors IXa and Xa
    摘要:
    Modifications to the P4 moiety and pyrazole C3 substituent of factor Xa inhibitor SN-429 provided several new compounds, which are 5-10nM inhibitors of factor IXa. An X-ray crystal structure of one example complexed to factor IXa shows that these compounds adopt a similar binding mode to that previously observed with pyrazole inhibitors in the factor Xa active site both with regard to how the inhibitor binds and the position of Tyr99.
    DOI:
    10.1016/j.bmcl.2004.08.034
  • 作为产物:
    参考文献:
    名称:
    SAR and factor IXa crystal structure of a dual inhibitor of factors IXa and Xa
    摘要:
    Modifications to the P4 moiety and pyrazole C3 substituent of factor Xa inhibitor SN-429 provided several new compounds, which are 5-10nM inhibitors of factor IXa. An X-ray crystal structure of one example complexed to factor IXa shows that these compounds adopt a similar binding mode to that previously observed with pyrazole inhibitors in the factor Xa active site both with regard to how the inhibitor binds and the position of Tyr99.
    DOI:
    10.1016/j.bmcl.2004.08.034
点击查看最新优质反应信息