2-Methyl-2-[4-[2-[4-[(E)-3-phenylprop-2-enoyl]phenoxy]ethyl]phenoxy]propanoic acid | 1415609-00-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: 2-Methyl-2-[4-[2-[4-[(E)-3-phenylprop-2-enoyl]phenoxy]ethyl]phenoxy]propanoic acid
• 英文别名: 2-methyl-2-[4-[2-[4-[(E)-3-phenylprop-2-enoyl]phenoxy]ethyl]phenoxy]propanoic acid
• CAS: 1415609-00-5
• 化学式: C₂₇H₂₆O₅
• 分子量: 430.5
• InChiKey: DYZWQRFFNWBPHH-LICLKQGHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  32
• 可旋转键数：
  10
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  72.8
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  ethyl 2-[4-(2-hydroxyethyl)phenoxy]-2-methylpropanoate 在 偶氮二甲酸二异丙酯 、 三苯基膦 、 sodium hydroxide 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 生成 2-Methyl-2-[4-[2-[4-[(E)-3-phenylprop-2-enoyl]phenoxy]ethyl]phenoxy]propanoic acid
  参考文献：
  名称：

  Synthesis and structure–activity relationships of fibrate-based analogues inside PPARs

  摘要：

  In an effort to develop safe and efficacious compounds for the treatment of metabolic disorders, new compounds based on a combination of clofibric acid, the active metabolite of clofibrate, and lipophilic groups derived from natural products chalcone and stilbene were synthesised. Some of them were found to be active at micromolar concentrations only on PPAR alpha or PPAR gamma, while others were identified as dual agonists PPAR alpha/gamma. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.09.111

文献信息

• Synthesis and structure–activity relationships of fibrate-based analogues inside PPARs
  作者：Letizia Giampietro、Alessandra D’Angelo、Antonella Giancristofaro、Alessandra Ammazzalorso、Barbara De Filippis、Marialuigia Fantacuzzi、Pasquale Linciano、Cristina Maccallini、Rosa Amoroso

  DOI：10.1016/j.bmcl.2012.09.111

  日期：2012.12

  In an effort to develop safe and efficacious compounds for the treatment of metabolic disorders, new compounds based on a combination of clofibric acid, the active metabolite of clofibrate, and lipophilic groups derived from natural products chalcone and stilbene were synthesised. Some of them were found to be active at micromolar concentrations only on PPAR alpha or PPAR gamma, while others were identified as dual agonists PPAR alpha/gamma. (C) 2012 Elsevier Ltd. All rights reserved.