1-palmitoyl-2-hydroxy-sn-glycero-3-phosphatidyl-(2-trimethylsilanylethoxycarbonylamino)ethanol | 590386-23-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 甘油磷脂
• 英文名称: 1-palmitoyl-2-hydroxy-sn-glycero-3-phosphatidyl-(2-trimethylsilanylethoxycarbonylamino)ethanol
• CAS: 590386-23-5
• 化学式: C₂₇H₅₆NO₉PSi
• 分子量: 597.802
• InChiKey: SRTMUQGPCIMQJQ-RUZDIDTESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.57
• 重原子数：
  39.0
• 可旋转键数：
  26.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.93
• 拓扑面积：
  140.62
• 氢给体数：
  3.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  1-palmitoyl-2-hydroxy-sn-glycero-3-phosphatidyl-(2-trimethylsilanylethoxycarbonylamino)ethanol 在 4-二甲氨基吡啶 、 Montmorillonite K₁₀ 、 四丁基氟化铵 、 臭氧 、 N,N'-二环己基碳二亚胺 作用下， 以 四氢呋喃 、 甲醇 、 氯仿 为溶剂， 反应 96.75h， 生成 1-palmitoyl-2-(5,5-dimethoxy-valeroyl)-sn-glycero-3-phosphatidylethanolamine
  参考文献：
  名称：

  Total Syntheses of Bioactive Oxidized Ethanolamine Phospholipids

  摘要：

  GraphicsTruncated ethanolamine phospholipids containing aldehyde functionality, e.g. OVPE, and the corresponding acids, are generated by oxidative cleavage of polyunsaturated phospholipids. To confirm their identities and facilitate studies of the chemistry and biological actions of these analogues of biologically active phosphatidylcholines, e.g. OVPC, total syntheses were developed. An efficient general strategy was used that features selective N-protection of 2-lysophosphatidylethanolamine, and generation of the target compounds by mild deprotection of stable precursors.

  DOI：

  10.1021/ol034729z
• 作为产物：
  描述：

  对硝基苯基三甲基硅乙基碳酸酯 、 1-棕榈-sn-甘油-3-磷酸乙醇胺 在 sodium carbonate 作用下， 反应 48.0h， 以73%的产率得到1-palmitoyl-2-hydroxy-sn-glycero-3-phosphatidyl-(2-trimethylsilanylethoxycarbonylamino)ethanol
  参考文献：
  名称：

  Total Syntheses of Bioactive Oxidized Ethanolamine Phospholipids

  摘要：

  GraphicsTruncated ethanolamine phospholipids containing aldehyde functionality, e.g. OVPE, and the corresponding acids, are generated by oxidative cleavage of polyunsaturated phospholipids. To confirm their identities and facilitate studies of the chemistry and biological actions of these analogues of biologically active phosphatidylcholines, e.g. OVPC, total syntheses were developed. An efficient general strategy was used that features selective N-protection of 2-lysophosphatidylethanolamine, and generation of the target compounds by mild deprotection of stable precursors.

  DOI：

  10.1021/ol034729z