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[4-Cyano-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridin-2-yl-methyl]-triphenyl-phosphonium chloride

中文名称
——
中文别名
——
英文名称
[4-Cyano-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridin-2-yl-methyl]-triphenyl-phosphonium chloride
英文别名
[4-cyano-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridin-2-yl-methyl]-triphenyl phosponium chloride;[4-cyano-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridin-2-ylmethyl]-triphenyl-phosphonium chloride;[4-cyano-6-[4-ethoxy-3-(trifluoromethyl)phenyl]-1H-imidazo[4,5-c]pyridin-2-yl]methyl-triphenylphosphanium;chloride
[4-Cyano-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridin-2-yl-methyl]-triphenyl-phosphonium chloride化学式
CAS
——
化学式
C35H27F3N4OP*Cl
mdl
——
分子量
643.048
InChiKey
PVCXKJLPXVDCHK-UHFFFAOYSA-M
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):
    4.41
  • 重原子数:
    45
  • 可旋转键数:
    8
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    74.6
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

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文献信息

  • 6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile derivatives
    申请人:Cai Jiaqiang
    公开号:US20070179138A1
    公开(公告)日:2007-08-02
    The present invention relates to 6-phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile derivatives having the general Formula I wherein each of the substituents is given the definition as set forth in the specification and claims, pharmaceutical compositions comprising the same as well as to the use of these derivatives for the preparation of a medicament for the treatment of cathepsin S and/or cathepsin K related diseases such as osteoporosis, atherosclerosis, inflammation and immune disorders, such as rheumatoid arthritis, and chronic pain, such as neuropathic pain.
    本发明涉及具有通式I的6-苯基-1H-咪唑[4,5-c]吡啶-4-碳腈衍生物,其中每个取代基的定义如规范和权利要求中所述,包括含有这些衍生物的药物组合物,以及利用这些衍生物制备用于治疗与cathepsin S和/或cathepsin K相关疾病的药物,如骨质疏松症、动脉粥样硬化、炎症和免疫紊乱,如类风湿性关节炎,以及慢性疼痛,如神经病理性疼痛。
  • 6-phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile derivatives
    申请人:N.V. Organon
    公开号:US07687515B2
    公开(公告)日:2010-03-30
    The present invention relates to 6-phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile derivatives having the general Formula I wherein each of the substituents is given the definition as set forth in the specification and claims, pharmaceutical compositions comprising the same as well as to the use of these derivatives for the preparation of a medicament for the treatment of cathepsin S and/or cathepsin K related diseases such as osteoporosis, atherosclerosis, inflammation and immune disorders, such as rheumatoid arthritis, and chronic pain, such as neuropathic pain.
    本发明涉及具有一般式I的6-苯基-1H-咪唑[4,5-c]吡啶-4-碳腈衍生物,其中每个取代基的定义如规范和权利要求中所述,以及包含它们的制药组合物,以及利用这些衍生物制备治疗与cathepsin S和/或cathepsin K相关的疾病,如骨质疏松症、动脉粥样硬化、炎症和免疫紊乱,如类风湿性关节炎和慢性疼痛,如神经病理性疼痛的药物的用途。
  • 6-PHENYL-1H-IMIDAZO[4, 5-C]PYRIDINE-4-CARBONITRILE DERIVATIVES AS CATHEPSIN K AND S INHIBITORS
    申请人:N.V. Organon
    公开号:EP1979351A1
    公开(公告)日:2008-10-15
  • US7687515B2
    申请人:——
    公开号:US7687515B2
    公开(公告)日:2010-03-30
  • [EN] 6-PHENYL-1H-IMIDAZO[4, 5-C]PYRIDINE-4-CARBONITRILE DERIVATIVES AS CATHEPSIN K AND S INHIBITORS<br/>[FR] DERIVES DU 6-PHENYL-1H-IMIDAZO[4, 5-C]PYRIDINE-4-CARBONITRILE UTILISES EN TANT QU'INHIBITEURS DE LA CATHEPSINE K ET S
    申请人:ORGANON NV
    公开号:WO2007080191A1
    公开(公告)日:2007-07-19
    [EN] The present invention relates to 6-phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile derivatives having the general Formula (I), to pharmaceutical compositions comprising the same as well as to the use of these derivatives for the preparation of a medicament for the treatment of cathepsin S and/or cathepsin K related diseases such as osteoporosis, atherosclerosis, inflammation and immune disorders, such as rheumatoid arthritis, and chronic pain, such as neuropathic pain.
    [FR] La présente invention concerne des dérivés du 6-phényl-1H-imidazo[4,5-c]pyridine-4-carbonitrile de formule générale (I), des compositions pharmaceutiques comprenant ces dérivés et l'utilisation de ces derniers pour la préparation d'un médicament destiné au traitement de maladies associées à la cathepsine S et/ou à la cathepsine K, telles que l'ostéoporose, l'athérosclérose, l'inflammation et les troubles immunitaires tels que la polyarthrite rhumatoïde, ainsi que la douleur chronique, telle que la douleur neuropathique.
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