(6bS)-8-acetyl-2-benzyl-6,9-dihydroxy-3,3,6b-trimethyl-[1]benzofuro[2,3-f][1,3]benzoxazine-1,7-dione | 1227077-72-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶嗪类
• 英文名称: (6bS)-8-acetyl-2-benzyl-6,9-dihydroxy-3,3,6b-trimethyl-[1]benzofuro[2,3-f][1,3]benzoxazine-1,7-dione
• CAS: 1227077-72-6
• 化学式: C₂₆H₂₃NO₇
• 分子量: 461.471
• InChiKey: WWCVBPLSLSEXNZ-AREMUKBSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  34
• 可旋转键数：
  3
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  113
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  C₃₃H₂₉NO₇ 在 1% Pd/C 、 氢气 作用下， 以 乙醇 、 乙酸乙酯 为溶剂， 反应 6.0h， 以41%的产率得到(6bS)-8-acetyl-2-benzyl-6,9-dihydroxy-3,3,6b-trimethyl-[1]benzofuro[2,3-f][1,3]benzoxazine-1,7-dione
  参考文献：
  名称：

  Discovery of a novel selective PPARγ modulator from (−)-Cercosporamide derivatives

  摘要：

  In an investigation of (-)-Cercosporamide derivatives with a plasma glucose-lowering effect, we found that N-benzylcarboxamide derivative 4 was a partial agonist of PPAR gamma. A SAR study of the substituents on carboxamide nitrogen afforded the N-(1-naphthyl) methylcarboxamide derivative 23 as the most potent selective PPAR gamma modulator. An X-ray crystallography study revealed that compound 23 bounded to the PPAR gamma ligand binding domain in a unique way without any interaction with helix12. Compound 23 displayed a potent plasma glucose-lowering effect in db/db mice without the undesirable increase in body fluid and heart weight that is typically observed when PPAR gamma full agonists are administrated. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.02.073

文献信息

• Discovery of a novel selective PPARγ modulator from (−)-Cercosporamide derivatives
  作者：Akihiro Furukawa、Tsuyoshi Arita、Susumu Satoh、Kenji Wakabayashi、Shinko Hayashi、Yumi Matsui、Kazushi Araki、Masanori Kuroha、Jun Ohsumi

  DOI：10.1016/j.bmcl.2010.02.073

  日期：2010.4

  In an investigation of (-)-Cercosporamide derivatives with a plasma glucose-lowering effect, we found that N-benzylcarboxamide derivative 4 was a partial agonist of PPAR gamma. A SAR study of the substituents on carboxamide nitrogen afforded the N-(1-naphthyl) methylcarboxamide derivative 23 as the most potent selective PPAR gamma modulator. An X-ray crystallography study revealed that compound 23 bounded to the PPAR gamma ligand binding domain in a unique way without any interaction with helix12. Compound 23 displayed a potent plasma glucose-lowering effect in db/db mice without the undesirable increase in body fluid and heart weight that is typically observed when PPAR gamma full agonists are administrated. (C) 2010 Elsevier Ltd. All rights reserved.