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2-chloro-5-(1-methyl-1H-pyrazol-3-yl)-N-(1-phenyl-3-pyridin-4-yl-1H-pyrazol-5-yl)-4-(trifluoromethyl)benzamide

中文名称
——
中文别名
——
英文名称
2-chloro-5-(1-methyl-1H-pyrazol-3-yl)-N-(1-phenyl-3-pyridin-4-yl-1H-pyrazol-5-yl)-4-(trifluoromethyl)benzamide
英文别名
2-chloro-5-(1-methylpyrazol-3-yl)-N-(2-phenyl-5-pyridin-4-ylpyrazol-3-yl)-4-(trifluoromethyl)benzamide
2-chloro-5-(1-methyl-1H-pyrazol-3-yl)-N-(1-phenyl-3-pyridin-4-yl-1H-pyrazol-5-yl)-4-(trifluoromethyl)benzamide化学式
CAS
——
化学式
C26H18ClF3N6O
mdl
——
分子量
522.9
InChiKey
YPTJLKAUNVFXEA-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):
    5.1
  • 重原子数:
    37
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    77.6
  • 氢给体数:
    1
  • 氢受体数:
    7

文献信息

  • [EN] TrkA KINASE INHIBITORS,COMPOSITIONS AND METHODS THEREOF<br/>[FR] INHIBITEURS DE LA KINASE TRKA, COMPOSITIONS ET MÉTHODES ASSOCIÉES
    申请人:MERCK SHARP & DOHME
    公开号:WO2015143653A1
    公开(公告)日:2015-10-01
    The present invention is directed to substituted five membered heteroaryl benzamide compounds compounds of formula (I), which are tropomyosin-related kinase (Trk) family protein kinase inhibitors, and hence are useful in the treatment of pain, inflammation, cancer, restenosis, atherosclerosis, psoriasis, thrombosis, a disease, disorder, injury, or malfunction relating to dysmyelination or demyelination or a disease or disorder associated with abnormal activities of nerve growth factor (NGF) receptor TrkA.
    本发明涉及一种替代的五元杂环芳基苯甲酰胺化合物,化学式为(I),它们是肌动蛋白相关激酶(Trk)家族蛋白激酶抑制剂,因此在治疗疼痛、炎症、癌症、再狭窄、动脉粥样硬化、屑病、血栓形成、与失髓鞘形成或脱髓鞘有关的疾病、紊乱、损伤或功能障碍,或与神经生长因子(NGF)受体TrkA的异常活动有关的疾病或紊乱中具有用处。
  • TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF
    申请人:Merck Sharp & Dohme Corp.
    公开号:EP3122343A2
    公开(公告)日:2017-02-01
  • TrKA Kinase Inhibitors, Compositions and Methods Thereof
    申请人:MITCHELL Helen
    公开号:US20170158698A1
    公开(公告)日:2017-06-08
    The present invention is directed to substituted five membered heteroaryl benzamide compounds of formula (I) (Formula (I)) which are tropomyosin-related kinase (Trk) family protein kinase inhibitors, and hence are useful in the treatment of pain, inflammation, cancer, restenosis, atherosclerosis, psoriasis, thrombosis, a disease, disorder, injury, or malfunction relating to dysmyelination or demyelination or a disease or disorder associated with abnormal activities of nerve growth factor (NGF) receptor TrkA.
  • US9914736B2
    申请人:——
    公开号:US9914736B2
    公开(公告)日:2018-03-13
  • [EN] TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF<br/>[FR] INHIBITEURS DE LA KINASE TRKA, COMPOSITIONS EN CONTENANT ET MÉTHODES ASSOCIÉES
    申请人:MERCK SHARP & DOHME
    公开号:WO2015148350A2
    公开(公告)日:2015-10-01
    The present invention is directed to substituted five membered heteroaryl benzamide compounds of formula (I) (Formula (I)) which are tropomyosin-related kinase (Trk) family protein kinase inhibitors, and hence are useful in the treatment of pain, inflammation, cancer, restenosis, atherosclerosis, psoriasis, thrombosis, a disease, disorder, injury, or malfunction relating to dysmyelination or demyelination or a disease or disorder associated with abnormal activities of nerve growth factor (NGF) receptor TrkA.
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