3-[2-[3-[2-[2-[2-[2-[[(3R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]ethoxy]ethoxy]ethoxy]ethoxy]propoxy]-3,4,5,6-tetrakis(3-methylsulfonyloxypropoxy)cyclohexyl]oxypropyl methanesulfonate | 1245938-20-8

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: 3-[2-[3-[2-[2-[2-[2-[[(3R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]ethoxy]ethoxy]ethoxy]ethoxy]propoxy]-3,4,5,6-tetrakis(3-methylsulfonyloxypropoxy)cyclohexyl]oxypropyl methanesulfonate
• CAS: 1245938-20-8
• 化学式: C₆₄H₁₁₈O₂₆S₅
• 分子量: 1463.96
• InChiKey: YMDXFVVGLPPPFI-KGWCQIBXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7
• 重原子数：
  95
• 可旋转键数：
  53
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.97
• 拓扑面积：
  360
• 氢给体数：
  0
• 氢受体数：
  26

反应信息

• 作为反应物：
  描述：

  3-[2-[3-[2-[2-[2-[2-[[(3R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]ethoxy]ethoxy]ethoxy]ethoxy]propoxy]-3,4,5,6-tetrakis(3-methylsulfonyloxypropoxy)cyclohexyl]oxypropyl methanesulfonate 在 sodium iodide 作用下， 以 丁酮 为溶剂， 生成
  参考文献：
  名称：

  Novel synthetic LPDs consisting of different cholesterol derivatives for gene transfer into hepatocytes

  摘要：

  In the present study, LPDs composing of a series of novel synthetic cholesterylated derivatives bearing a cluster of galactose residues and different spacer lengths were prepared for performing target gene delivery to hepatocytes and their physiochemical properties as well as gene transfer efficiency were investigated. In agreement with the "clustering effect" known to occur with more complex oligomeric structures, the addition of galactose residues under optimized spatial arrangement condition invariably increased the transfect efficiency into hepatoma cells, which can be owed to the sufficient binding of galactose ligands to the ASGPR on hepatocytes. However, the gene transfer ability to hepatocytes was not always improved with extended spacer arms, suggesting a spatial binding sites arrangement of the receptor. Moreover, our research has established galactosylated LPDs, specifically, LPDIIb, LPDIIIc, and LPDIVe as potential vectors to deliver special genes into hepatocytes with low toxicity, combining the condensing effect of protamine and the targeting capability of cholesterylated thiogalactosides.

  DOI：

  10.3109/10611860903548370
• 作为产物：
  描述：

  11-(5-cholesten-3α-yloxy)-3n³₉-trioxaundecan-1-ol 、 3-[2,3,4,5,6-Pentakis(3-methylsulfonyloxypropoxy)cyclohexyl]oxypropyl methanesulfonate 在 sodium hydride 作用下， 生成 3-[2-[3-[2-[2-[2-[2-[[(3R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]ethoxy]ethoxy]ethoxy]ethoxy]propoxy]-3,4,5,6-tetrakis(3-methylsulfonyloxypropoxy)cyclohexyl]oxypropyl methanesulfonate
  参考文献：
  名称：

  Novel synthetic LPDs consisting of different cholesterol derivatives for gene transfer into hepatocytes

  摘要：

  In the present study, LPDs composing of a series of novel synthetic cholesterylated derivatives bearing a cluster of galactose residues and different spacer lengths were prepared for performing target gene delivery to hepatocytes and their physiochemical properties as well as gene transfer efficiency were investigated. In agreement with the "clustering effect" known to occur with more complex oligomeric structures, the addition of galactose residues under optimized spatial arrangement condition invariably increased the transfect efficiency into hepatoma cells, which can be owed to the sufficient binding of galactose ligands to the ASGPR on hepatocytes. However, the gene transfer ability to hepatocytes was not always improved with extended spacer arms, suggesting a spatial binding sites arrangement of the receptor. Moreover, our research has established galactosylated LPDs, specifically, LPDIIb, LPDIIIc, and LPDIVe as potential vectors to deliver special genes into hepatocytes with low toxicity, combining the condensing effect of protamine and the targeting capability of cholesterylated thiogalactosides.

  DOI：

  10.3109/10611860903548370