1-palmitoyl-2-succinoyl-sn-glycero-3-phosphatidyl-(2-tert-butoxycarbonylamino)ethanol | 590386-42-8

• 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-succinoyl-sn-glycero-3-phosphatidyl-(2-tert-butoxycarbonylamino)ethanol
• CAS: 590386-42-8
• 化学式: C₃₀H₅₆NO₁₂P
• 分子量: 653.748
• InChiKey: JYKRZNUTKBCUJJ-RUZDIDTESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.45
• 重原子数：
  44.0
• 可旋转键数：
  27.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  183.99
• 氢给体数：
  3.0
• 氢受体数：
  10.0

反应信息

• 作为反应物：
  描述：

  1-palmitoyl-2-succinoyl-sn-glycero-3-phosphatidyl-(2-tert-butoxycarbonylamino)ethanol 在 三氟乙酸 作用下， 反应 0.5h， 以70%的产率得到1-palmitoyl-2-succinoyl-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：

  1-palmitoyl-2-(4-pentenoyl)-sn-glycero-3-phosphatidyl-(2-tert-butoxycarbonylamino)ethanol 在 sodium chlorite 、 disodium hydrogenphosphate 、 2-甲基-2-丁烯 、 臭氧 作用下， 以 四氢呋喃 、 甲醇 、 氯仿 、 水 、 叔丁醇 为溶剂， 反应 2.0h， 生成 1-palmitoyl-2-succinoyl-sn-glycero-3-phosphatidyl-(2-tert-butoxycarbonylamino)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