摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

5-(Methylsulfonyl)-1-pentanol | 558466-07-2

中文名称
——
中文别名
——
英文名称
5-(Methylsulfonyl)-1-pentanol
英文别名
5-methylsulfonylpentan-1-ol
5-(Methylsulfonyl)-1-pentanol化学式
CAS
558466-07-2
化学式
C6H14O3S
mdl
——
分子量
166.241
InChiKey
GYWGTIUZWRJGPS-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):
    0
  • 重原子数:
    10
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    62.8
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Substituted Pyridine Compound
    申请人:Nakamura Tsuyoshi
    公开号:US20130109653A1
    公开(公告)日:2013-05-02
    The present invention provides a substituted pyridine compound or a pharmacologically acceptable salt thereof which has excellent CETP inhibition activity and is useful as a medicament. The present invention provides a compound represented by a general formula (I), wherein R 1 is H, optionally substituted alkyl, OH, optionally substituted alkoxy, alkylsulfonyl, optionally substituted amino, carboxy, optionally substituted carbonyl, CN, halogeno, optionally substituted phenyl, optionally substituted aromatic heterocyclyl, optionally substituted saturated heterocyclyl, optionally substituted saturated heterocyclyloxy or optionally substituted saturated heterocyclylcarbonyl, etc., and the like.
    本发明提供了一种取代吡啶化合物或其药理学上可接受的盐,具有优异的CETP抑制活性,并可用作药物。本发明提供了一种由通式(I)表示的化合物,其中R1为H,可选地取代的烷基,OH,可选地取代的烷氧基,烷基磺酰基,可选地取代的氨基,羧基,可选地取代的羰基,CN,卤素,可选地取代的苯基,可选地取代的芳香杂环基,可选地取代的饱和杂环基,可选地取代的饱和杂环氧基或可选地取代的饱和杂环羰基等。
  • Beta-amyloid protein production. secretion inhibitor
    申请人:Yasukouchi Takanori
    公开号:US20050234109A1
    公开(公告)日:2005-10-20
    Provided are novel compounds having an inhibitory activity against production or secretion of β-amyloid protein. They embrace compounds represented by the following formula (1): and capable of being replaced with a variety of substituents; and salts thereof, and solvates of any one of them.
    提供了一种新型化合物,具有抑制β-淀粉样蛋白产生或分泌的活性。它们包括由以下公式(1)表示的化合物:并且能够被各种取代基所替换;以及它们的盐和任何一个溶剂化物。
  • BETA-AMYLOID PROTEIN PRODUCTION/SECRETION INHIBITORS
    申请人:YASUKOUCHI Takanori
    公开号:US20070293495A1
    公开(公告)日:2007-12-20
    Provided are novel compounds having an inhibitory activity against production or secretion of β-amyloid protein. They embrace compounds represented by the following formula (1): and capable of being replaced with a variety of substituents; and salts thereof, and solvates of any one of them.
    提供了一些新化合物,具有抑制β-淀粉样蛋白的产生或分泌活性。它们包括以下式子(1)所代表的化合物:并且可以被各种取代基所替换;以及它们的盐和任何一个的溶剂化物。
  • β-amyloid protein production/secretion inhibitor
    申请人:Daiichi Pharmaceutical Co., Ltd.
    公开号:US07399775B2
    公开(公告)日:2008-07-15
    Provided are novel compounds having an inhibitory activity against production or secretion of β-amyloid protein. They embrace compounds represented by the following formula (1): and capable of being replaced with a variety of substituents; and salts thereof, and solvates of any one of them.
    提供了一种新型化合物,具有抑制β-淀粉样蛋白产生或分泌的活性。它们包括由以下式子(1)表示的化合物:并且可以被各种取代基替换;以及它们的盐和任何一个溶剂化物。
  • Substituted PyridineCompound
    申请人:Nakamura Tsuyoshi
    公开号:US20140005143A2
    公开(公告)日:2014-01-02
    The present invention provides a substituted pyridine compound or a pharmacologically acceptable salt thereof which has excellent CETP inhibition activity and is useful as a medicament. The present invention provides a compound represented by a general formula (I), wherein R 1 is H, optionally substituted alkyl, OH, optionally substituted alkoxy, alkylsulfonyl, optionally substituted amino, carboxy, optionally substituted carbonyl, CN, halogeno, optionally substituted phenyl, optionally substituted aromatic heterocyclyl, optionally substituted saturated heterocyclyl, optionally substituted saturated heterocyclyloxy or optionally substituted saturated heterocyclylcarbonyl, etc., and the like.
    本发明提供了一种替代吡啶化合物或其药学上可接受的盐,具有优异的CETP抑制活性,并可用作药物。本发明提供了一种由通式(I)表示的化合物,其中R1为H、可选取代烷基、OH、可选取代烷氧基、烷基磺酰基、可选取代氨基、羧基、可选取代羰基、CN、卤素、可选取代苯基、可选取代芳香杂环基、可选取代饱和杂环基、可选取代饱和杂环氧基或可选取代饱和杂环羰基等。
查看更多