| 634908-38-6

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• CAS: 634908-38-6
• 化学式: C₃₆H₆₅N₃O₄Si
• 分子量: 632.015
• InChiKey: MVVWQZMSRCTSCS-BZGIPGOBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.49
• 重原子数：
  44.0
• 可旋转键数：
  21.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  89.55
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 以72%的产率得到[(E)-(2S,3R)-2-(2,2-Dimethyl-propionylamino)-3-hydroxy-octadec-4-enyl]-carbamic acid pyridin-4-ylmethyl ester
  参考文献：
  名称：

  Biological evaluation of sphingomyelin analogues as inhibitors of sphingomyelinase

  摘要：

  Seeking neutral sphingomyelinase inhibitors, we designed and synthesized hydrolytically stable analogues of sphingomyelin. These novel analogues replace the phosphodiester moiety of sphingomyelin with carbamate and urea moiety, resulting in inhibition of neutral sphingomyelinase. Compound I prevented ceramide generation and apoptotic neuronal cell death in a model of ischemia based on organotypic hippocampal slice cultures. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.08.020
• 作为产物：
  描述：

  N-[(E)-(1S,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-(hydroxyimino-methyl)-heptadec-3-enyl]-2,2-dimethyl-propionamide 在 吡啶 、 sodium tetrahydroborate 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 为溶剂， 生成
  参考文献：
  名称：

  Biological evaluation of sphingomyelin analogues as inhibitors of sphingomyelinase

  摘要：

  Seeking neutral sphingomyelinase inhibitors, we designed and synthesized hydrolytically stable analogues of sphingomyelin. These novel analogues replace the phosphodiester moiety of sphingomyelin with carbamate and urea moiety, resulting in inhibition of neutral sphingomyelinase. Compound I prevented ceramide generation and apoptotic neuronal cell death in a model of ischemia based on organotypic hippocampal slice cultures. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.08.020