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3-methyl-2-{[(3R,6R)-6-methyl-1-{[2-(1,3-thiazol-2-yl)thiophen-3-yl]carbonyl}piperidin-3-yl]oxy} pyridin-4-carbonitrile | 1607428-37-4

中文名称
——
中文别名
——
英文名称
3-methyl-2-{[(3R,6R)-6-methyl-1-{[2-(1,3-thiazol-2-yl)thiophen-3-yl]carbonyl}piperidin-3-yl]oxy} pyridin-4-carbonitrile
英文别名
US9546152, example 32;3-methyl-2-[(3R,6R)-6-methyl-1-[2-(1,3-thiazol-2-yl)thiophene-3-carbonyl]piperidin-3-yl]oxypyridine-4-carbonitrile
3-methyl-2-{[(3R,6R)-6-methyl-1-{[2-(1,3-thiazol-2-yl)thiophen-3-yl]carbonyl}piperidin-3-yl]oxy} pyridin-4-carbonitrile化学式
CAS
1607428-37-4
化学式
C21H20N4O2S2
mdl
——
分子量
424.547
InChiKey
CXPNMJKLLBPCNK-CZUORRHYSA-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):
    3.8
  • 重原子数:
    29
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    136
  • 氢给体数:
    0
  • 氢受体数:
    7

文献信息

  • [EN] 2-PYRIDYLOXY-3-SUBSTITUTED-4-NITRILE OREXIN RECEPTOR ANTAGONISTS<br/>[FR] ANTAGONISTES DU RÉCEPTEUR DE LA 2-PYRIDYLOXY-3-SUBSTITUÉE-4-NITRILE ORÉXINE
    申请人:MERCK SHARP & DOHME
    公开号:WO2014066196A1
    公开(公告)日:2014-05-01
    The present invention is directed to 2-pyridyloxy-3-substituted-4-nitrile compounds which are antagonists of orexin receptors. The present invention is also directed to uses of the 2-pyridyloxy-3-substituted-4-nitrile compounds described herein in the treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to pharmaceutical compositions comprising these compounds. The present invention is also directed to uses of these pharmaceutical compositions in the prevention or treatment of such diseases in which orexin receptors are involved.
    本发明涉及2-吡啶氧基-3-取代-4-腈化合物,其是促进睡眠荷尔蒙受体的拮抗剂。本发明还涉及使用本文所述的2-吡啶氧基-3-取代-4-腈化合物在治疗或预防神经系统和精神疾病中的用途,其中涉及促进睡眠荷尔蒙受体。本发明还涉及包含这些化合物的制药组合物。本发明还涉及使用这些制药组合物在预防或治疗涉及促进睡眠荷尔蒙受体的疾病中的用途。
  • 2-PYRIDYLOXY-3-SUBSTITUTED-4-NITRILE OREXIN RECEPTOR ANTAGONISTS
    申请人:KUDUK Scott D.
    公开号:US20150291558A1
    公开(公告)日:2015-10-15
    The present invention is directed to 2-pyridyloxy-3-substituted-4-nitrile compounds which are antagonists of orexin receptors. The present invention is also directed to uses of the 2-pyridyloxy-3-substituted-4-nitrile compounds described herein in the treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to pharmaceutical compositions comprising these compounds. The present invention is also directed to uses of these pharmaceutical compositions in the prevention or treatment of such diseases in which orexin receptors are involved.
    本发明涉及2-吡啶氧基-3-取代-4-腈化合物,其为促进睡眠激素受体的拮抗剂。本发明还涉及使用本文所述的2-吡啶氧基-3-取代-4-腈化合物在治疗或预防神经和精神障碍和疾病中的应用,其中促进睡眠激素受体参与其中。本发明还涉及包含这些化合物的药物组合物。本发明还涉及使用这些药物组合物在预防或治疗促进睡眠激素受体参与的疾病中的应用。
  • 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 Santé et de la Recherche Médicale)
    公开号:EP3223803A1
    公开(公告)日:2017-10-04
  • 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:EP3218007A1
    公开(公告)日:2017-09-20
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