[(2R,3R,4R,5S,6S)-3-acetyloxy-2-(benzamidomethyl)-5-benzoyloxy-6-(2,5-dimethoxyphenyl)oxan-4-yl] benzoate | 1101835-40-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: [(2R,3R,4R,5S,6S)-3-acetyloxy-2-(benzamidomethyl)-5-benzoyloxy-6-(2,5-dimethoxyphenyl)oxan-4-yl] benzoate
• CAS: 1101835-40-8
• 化学式: C₃₇H₃₅NO₁₀
• 分子量: 653.686
• InChiKey: WEZWMQUFMRFDPK-BBZHULIZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.5
• 重原子数：
  48
• 可旋转键数：
  14
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  136
• 氢给体数：
  1
• 氢受体数：
  10

反应信息

• 作为产物：
  描述：

  [(2R,3R,4S,5S,6S)-2-(benzamidomethyl)-5-benzoyloxy-6-(2,5-dimethoxyphenyl)-3-hydroxyoxan-4-yl] benzoate 、 乙酸酐 在 吡啶 作用下， 以85%的产率得到[(2R,3R,4R,5S,6S)-3-acetyloxy-2-(benzamidomethyl)-5-benzoyloxy-6-(2,5-dimethoxyphenyl)oxan-4-yl] benzoate
  参考文献：
  名称：

  β-C-Glycosiduronic acids and β-C-glycosyl compounds: New PTP1B inhibitors

  摘要：

  beta-C-Glycosiduronic acid quinones and beta-C-glycosyl compounds have been synthesized as sugar-based PTP1B inhibitors. Benzoyl protected quinone derivatives (14 and 35) as well as aryl beta-C-glycosyl compounds (18, 22, 23 and 34) showed IC50 values of 0.77-5.27 mu M against PTP1B, with compounds 18 and 23 bearing an acidic function being the most potent. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.10.091

文献信息

• β-C-Glycosiduronic acids and β-C-glycosyl compounds: New PTP1B inhibitors
  作者：Li Lin、Qiang Shen、Guo-Rong Chen、Juan Xie

  DOI：10.1016/j.bmcl.2008.10.091

  日期：2008.12

  beta-C-Glycosiduronic acid quinones and beta-C-glycosyl compounds have been synthesized as sugar-based PTP1B inhibitors. Benzoyl protected quinone derivatives (14 and 35) as well as aryl beta-C-glycosyl compounds (18, 22, 23 and 34) showed IC50 values of 0.77-5.27 mu M against PTP1B, with compounds 18 and 23 bearing an acidic function being the most potent. (C) 2008 Elsevier Ltd. All rights reserved.