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(E)-3-(1,3-benzodioxol-4-yl)-N-(2-methyl-1,5-naphthyridin-4-yl)prop-2-enamide

中文名称
——
中文别名
——
英文名称
(E)-3-(1,3-benzodioxol-4-yl)-N-(2-methyl-1,5-naphthyridin-4-yl)prop-2-enamide
英文别名
——
(E)-3-(1,3-benzodioxol-4-yl)-N-(2-methyl-1,5-naphthyridin-4-yl)prop-2-enamide化学式
CAS
——
化学式
C19H15N3O3
mdl
——
分子量
333.3
InChiKey
SXHNGQOWRHXXOC-BQYQJAHWSA-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):
    2.7
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    73.3
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • Methods and pharmaceutical compositions for the treatment of cancer
    申请人:INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE)
    公开号:US10894042B2
    公开(公告)日:2021-01-19
    The present invention relates to methods and pharmaceutical compositions for the treatment of cancer. More particularly, the present invention relates to a method of treating cancer in subject in need thereof comprising administering the subject with a therapeutically effective amount of at least one OX1R antagonist.
    本发明涉及治疗癌症的方法和药物组合物。更具体地说,本发明涉及一种治疗有需要的受试者癌症的方法,该方法包括向受试者施用治疗有效量的至少一种 OX1R 拮抗剂。
  • USE OF OX1R ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY BOWEL DISEASES
    申请人:Inserm (Institut National De La Sante et de la Recherche Medicale)
    公开号:US20190083508A1
    公开(公告)日:2019-03-21
    The present invention relates to methods and pharmaceutical compositions for the treatment of inflammatory bowel diseases.
  • METHODS AND PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF AUTOIMMUNE INFLAMMATORY
    申请人:INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCJAE MÉDICALE
    公开号:US20190151304A1
    公开(公告)日:2019-05-23
    The present invention relates to methods and pharmaceutical compositions for the treatment of autoimmune inflammatory diseases. The inventors showed that orexin receptor antagonists have anti-inflammatory properties. Indeed, these compounds are antagonist for OX1R-mediated calcium mobilization but a full agonist for OX1R-mediated mitochondrial apoptosis, which is the mechanism involved in the improvement of resolution of inflammation observed in the models of colitis, multiple sclerosis and pancreatitis. In particular, the present invention relates to a method of treating an autoimmune inflammatory disease in a subject in need thereof comprising administering to the subject a therapeutically effective amount of at least one OX1R antagonist.
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