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(2S)-2-fluoropropan-1-ol | 877822-87-2

中文名称
——
中文别名
——
英文名称
(2S)-2-fluoropropan-1-ol
英文别名
——
(2S)-2-fluoropropan-1-ol化学式
CAS
877822-87-2
化学式
C3H7FO
mdl
——
分子量
78.0864
InChiKey
WKXZJCKWUCBECD-VKHMYHEASA-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):
    0.3
  • 重原子数:
    5
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • SULFONAMIDE COMPOUNDS OR SALTS THEREOF
    申请人:Kubota Hideki
    公开号:US20110201616A1
    公开(公告)日:2011-08-18
    [Object] A compound which is useful as an EP1 receptor antagonist is provided. [Means for Solution] The present inventors investigated EP1 receptor antagonists, and confirmed that a compound having a sulfonamide structure, in which the nitrogen atom of the sulfonamide structure is substituted with 2-fluoropropyl group, 3-fluoro-2-methylpropyl group or the like, has a potent EP1 receptor antagonistic action, thereby completing the present invention. The sulfonamide compound of the present invention has a potent EP1 receptor antagonistic action and can be used as an agent for preventing and/or treating a lower urinary tract symptom or the like.
    [物件] 提供了一种作为EP1受体拮抗剂有用的化合物。 [解决方案手段] 现有发明人研究了EP1受体拮抗剂,并确认具有磺酰胺结构的化合物,其中磺酰胺结构的氮原子被2-氟丙基基团,3-氟-2-甲基丙基基团或类似基团取代,具有强效的EP1受体拮抗作用,从而完成了本发明。本发明的磺酰胺化合物具有强效的EP1受体拮抗作用,可用作预防和/或治疗下尿路症状等剂。
  • Sulfonamide compounds or salts thereof
    申请人:Astellas Pharma Inc.
    公开号:US08314240B2
    公开(公告)日:2012-11-20
    [Object] A compound which is useful as an EP1 receptor antagonist is provided. [Means for Solution] The present inventors investigated EP1 receptor antagonists, and confirmed that a compound having a sulfonamide structure, in which the nitrogen atom of the sulfonamide structure is substituted with 2-fluoropropyl group, 3-fluoro-2-methylpropyl group or the like, has a potent EP1 receptor antagonistic action, thereby completing the present invention. The sulfonamide compound of the present invention has a potent EP1 receptor antagonistic action and can be used as an agent for preventing and/or treating a lower urinary tract symptom or the like.
    【物品】提供一种作为EP1受体拮抗剂有用的化合物。 【解决方案】本发明人调查了EP1受体拮抗剂,并确认一种具有磺酰胺结构的化合物,其中磺酰胺结构的氮原子被取代为2-氟丙基基团、3-氟-2-甲基丙基基团或类似基团,具有有效的EP1受体拮抗作用,从而完成了本发明。本发明的磺酰胺化合物具有有效的EP1受体拮抗作用,可用作预防和/或治疗下尿路症状等的药物。
  • PYRAZOLOQUINOLINE COMPOUND
    申请人:ASTELLAS PHARMA INC.
    公开号:US20130225553A1
    公开(公告)日:2013-08-29
    The present inventors have investigated a compound which has a PDE9-inhibiting action and is useful as an active ingredient for an agent for treating and/or preventing storage dysfunction, voiding dysfunction, bladder/urethral diseases, and the like, and thus, have found that a pyrazoloquinoline compound has a PDE9-inhibiting action, thereby completing the present invention.
    本发明者已经研究了一种具有PDE9抑制作用的化合物,并且可用作治疗和/或预防储存功能障碍,排尿功能障碍,膀胱/尿道疾病等制剂的活性成分。因此,发现一种吡唑喹啉化合物具有PDE9抑制作用,从而完成了本发明。
  • Pyrazoloquinoline compound
    申请人:Astellas Pharma Inc.
    公开号:US08822448B2
    公开(公告)日:2014-09-02
    The present inventors have investigated a compound which has a PDE9-inhibiting action and is useful as an active ingredient for an agent for treating and/or preventing storage dysfunction, voiding dysfunction, bladder/urethral diseases, and the like, and thus, have found that a pyrazoloquinoline compound has a PDE9-inhibiting action, thereby completing the present invention.
    本发明者研究了一种具有PDE9抑制作用的化合物,可用作治疗和/或预防储存功能障碍、排尿功能障碍、膀胱/尿道疾病等药物的活性成分,并因此发现一种吡唑喹啉化合物具有PDE9抑制作用,从而完成了本发明。
  • EP2305641
    申请人:——
    公开号:——
    公开(公告)日:——
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