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4-(5-trifluoromethyl-pyridin-2-ylsulfanyl)-benzaldehyde | 882985-35-5

中文名称
——
中文别名
——
英文名称
4-(5-trifluoromethyl-pyridin-2-ylsulfanyl)-benzaldehyde
英文别名
4-[5-(trifluoromethyl)pyridin-2-yl]sulfanylbenzaldehyde
4-(5-trifluoromethyl-pyridin-2-ylsulfanyl)-benzaldehyde化学式
CAS
882985-35-5
化学式
C13H8F3NOS
mdl
MFCD19528727
分子量
283.274
InChiKey
ZBMMWRJLFLRABX-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):
    3.6
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.076
  • 拓扑面积:
    55.3
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    对氟苯甲醛2-巯基-5-(三氟甲基)吡啶potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 18.0h, 以87%的产率得到4-(5-trifluoromethyl-pyridin-2-ylsulfanyl)-benzaldehyde
    参考文献:
    名称:
    Arylthiobenzylpiperidine derivatives
    摘要:
    这项发明涉及芳基硫代苯基哌啶衍生物,这些衍生物是MCH1受体的配体。该发明提供了一种包含该发明化合物的治疗有效量和药用载体的药物组合物。该发明还提供了一种通过混合该发明化合物的治疗有效量和药用载体制备的药物组合物。该发明进一步提供了一种制备药物组合物的方法,包括结合该发明化合物的治疗有效量和药用载体。该发明还提供了一种治疗患有抑郁症和/或焦虑症的受试者的方法,包括向受试者施用该发明化合物的治疗有效量。该发明还提供了一种治疗患有肥胖症的受试者的方法,包括向受试者施用该发明化合物的治疗有效量。
    公开号:
    US20060079523A1
点击查看最新优质反应信息

文献信息

  • Arylthiobenzylpiperidine Derivatives
    申请人:Marzabadi Mohammad R.
    公开号:US20080139555A1
    公开(公告)日:2008-06-12
    This invention is directed to Arylthiobenzylpiperidine derivatives which are ligands at the MCH1 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a pharmaceutical composition made by admixing a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of treating a subject suffering from depression and/or anxiety which comprises administering to the subject a therapeutically effective amount of a compound of the subject invention. This invention also provides a method of treating a subject suffering from obesity which comprises administering to the subject a therapeutically effective amount of a compound of the subject invention.
    本发明涉及芳基硫代苄基哌啶衍生物,其为MCH1受体的配体。本发明提供一种制备药物组合物的方法,包括将本发明化合物的治疗有效量与药学上可接受的载体混合。本发明还提供一种制备药物组合物的方法,包括将本发明化合物的治疗有效量与药学上可接受的载体混合。本发明还提供一种制备药物组合物的方法,包括将本发明化合物的治疗有效量与药学上可接受的载体混合。本发明还提供一种治疗抑郁症和/或焦虑症的方法,包括向患者施用本发明化合物的治疗有效量。本发明还提供一种治疗肥胖症的方法,包括向患者施用本发明化合物的治疗有效量。
  • EP1799223A4
    申请人:——
    公开号:EP1799223A4
    公开(公告)日:2008-01-23
  • ARYLTHIOBENZYLPIPERIDINE DERIVATES
    申请人:H.Lundbeck A/S
    公开号:EP1799223A2
    公开(公告)日:2007-06-27
  • US7329656B2
    申请人:——
    公开号:US7329656B2
    公开(公告)日:2008-02-12
  • [EN] ARYLTHIOBENZYLPIPERIDINE DERIVATES<br/>[FR] DERIVES D'ARYLTHIOBENZYLPIPERIDINE
    申请人:LUNDBECK & CO AS H
    公开号:WO2006041635A2
    公开(公告)日:2006-04-20
    This invention is directed to Arylthiobenzylpiperidine derivatives which are ligands at the MCH1 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a pharmaceutical composition made by admixing a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of treating a subject suffering from depression and/or anxiety which comprises administering to the subject a therapeutically effective amount of a compound of the subject invention. This invention also provides a method of treating a subject suffering from obesity which comprises administering to the subject a therapeutically effective amount of a compound of the subject invention.
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