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2-[6-[2-[4-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-oxazol-5-yl]propan-2-ylsulfanyl]-1-benzofuran-3-yl]acetic acid

中文名称
——
中文别名
——
英文名称
2-[6-[2-[4-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-oxazol-5-yl]propan-2-ylsulfanyl]-1-benzofuran-3-yl]acetic acid
英文别名
——
2-[6-[2-[4-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-oxazol-5-yl]propan-2-ylsulfanyl]-1-benzofuran-3-yl]acetic acid化学式
CAS
——
化学式
C24H20F3NO4S
mdl
——
分子量
475.5
InChiKey
NSBICDHFGBCYQA-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):
    5.8
  • 重原子数:
    33
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    102
  • 氢给体数:
    1
  • 氢受体数:
    9

文献信息

  • Fused heterocyclic derivates as ppar modulators
    申请人:Conner Eugene Scott
    公开号:US20060217374A1
    公开(公告)日:2006-09-28
    The present invention is directed to a method of treatment by modulating a peroxisome proliferator activated receptor by employing a compound of Structural Formula (I). The variables in I are defined herein. Also included are compounds, methods of making compounds, and pharmaceutical compositions. The compounds of the present invention are believed to be effective in treating and preventing Syndrome X, Type H diabetes, hyperglycemia, hyperlipidemia, obesity, coagaulopathy, hypertension, atherosclerosis, and other disorders related to Syndrome X and cardiovascular diseases.
    本发明涉及一种通过利用结构式(I)的化合物来调节过氧化物酶体增殖物激活受体进行治疗的方法。I中的变量在此定义。还包括化合物、制备化合物的方法和制药组合物。本发明的化合物被认为在治疗和预防综合征X、H型糖尿病、高血糖、高脂血症、肥胖症、凝血障碍、高血压、动脉粥样硬化和其他与综合征X和心血管疾病相关的疾病方面具有疗效。
  • FUSED HETEROCYCLIC DERIVATIVES AS PPAR MODULATORS
    申请人:ELI LILLY AND COMPANY
    公开号:EP1581521A1
    公开(公告)日:2005-10-05
  • US7528160B2
    申请人:——
    公开号:US7528160B2
    公开(公告)日:2009-05-05
  • [EN] FUSED HETEROCYCLIC DERIVATES AS PPAR MODULATORS<br/>[FR] DERIVES HETEROCYCLIQUES FUSIONNES UTILISES EN TANT QUE MODULATEURS PPAR
    申请人:LILLY CO ELI
    公开号:WO2004063190A1
    公开(公告)日:2004-07-29
    The present invention is directed to a method of treatment by modulating a peroxisome proliferator activated receptor by employing a compound of Structural Formula (I). The variables in I are defined herein. Also included are compounds, methods of making compounds, and pharmaceutical compositions. The compounds of the present invention are believed to be effective in treating and preventing Syndrome X, Type II diabetes, hyperglycemia, hyperlipidemia, obesity, coagaulopathy, hypertension, atherosclerosis, and other disorders related to Syndrome X and cardiovascular diseases.
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