2-[4-(4-chlorobenzoyl)phenoxy]-2-methyl-N-methylsulfonylpropanamide | 1415721-93-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-[4-(4-chlorobenzoyl)phenoxy]-2-methyl-N-methylsulfonylpropanamide
• CAS: 1415721-93-5
• 化学式: C₁₈H₁₈ClNO₅S
• 分子量: 395.864
• InChiKey: PWQAFTLRVOOHII-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  26
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  97.9
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  甲基磺酰胺 、 非诺贝特酸 在 4-二甲氨基吡啶 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 反应 24.25h， 以73%的产率得到2-[4-(4-chlorobenzoyl)phenoxy]-2-methyl-N-methylsulfonylpropanamide
  参考文献：
  名称：

  Fibrate-derived N-(methylsulfonyl)amides with antagonistic properties on PPARα

  摘要：

  The identification of novel PPAR ligands represents an attractive research to fully understand the complex biological pathways regulated by these receptors. Selective PPAR modulators, inverse agonists and antagonists of three PPAR isoforms could help to clarify biological effects on lipid and glucose homeostasis. Here we describe the identification of a group of N-(methylsulfonyl)amides, derived from PPAR alpha agonist carboxylic acids. Transactivation and FRET assay confirmed an antagonist behaviour on PPAR alpha for some of these compounds, with submicromolar IC50. A preliminary analysis on selectivity alpha/gamma revealed different profiles of inhibition or activation. (C) 2012 Published by Elsevier Masson SAS.

  DOI：

  10.1016/j.ejmech.2012.10.019

文献信息

• Fibrate-derived N-(methylsulfonyl)amides with antagonistic properties on PPARα
  作者：Alessandra Ammazzalorso、Alessandra D'Angelo、Antonella Giancristofaro、Barbara De Filippis、Mauro Di Matteo、Marialuigia Fantacuzzi、Letizia Giampietro、Pasquale Linciano、Cristina Maccallini、Rosa Amoroso

  DOI：10.1016/j.ejmech.2012.10.019

  日期：2012.12

  The identification of novel PPAR ligands represents an attractive research to fully understand the complex biological pathways regulated by these receptors. Selective PPAR modulators, inverse agonists and antagonists of three PPAR isoforms could help to clarify biological effects on lipid and glucose homeostasis. Here we describe the identification of a group of N-(methylsulfonyl)amides, derived from PPAR alpha agonist carboxylic acids. Transactivation and FRET assay confirmed an antagonist behaviour on PPAR alpha for some of these compounds, with submicromolar IC50. A preliminary analysis on selectivity alpha/gamma revealed different profiles of inhibition or activation. (C) 2012 Published by Elsevier Masson SAS.