1-cholesterylcarbonoyl-2-myristyl-rac-glycero-3-phosphocholine | 1085528-86-4

• 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: 1-cholesterylcarbonoyl-2-myristyl-rac-glycero-3-phosphocholine
• 英文别名: ChcMePC；[3-[[(3S,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]oxycarbonyloxy]-2-tetradecoxypropyl] 2-(trimethylazaniumyl)ethyl phosphate
• CAS: 1085528-86-4
• 化学式: C₅₀H₉₂NO₈P
• 分子量: 866.256
• InChiKey: PZISDTIKOZZSPM-OIWQZNLKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  14.8
• 重原子数：
  60
• 可旋转键数：
  31
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.94
• 拓扑面积：
  103
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  choline tetraphenyl borate 、 1-cholesterylcarbonoyl-2-myristyl-rac-glycero-3-phosphate 在 2,4,6-三异丙基苯磺酰氯 作用下， 以 吡啶 为溶剂， 生成 1-cholesterylcarbonoyl-2-myristyl-rac-glycero-3-phosphocholine
  参考文献：
  名称：

  Sterol-Modified Phospholipids: Cholesterol and Phospholipid Chimeras with Improved Biomembrane Properties

  摘要：

  We synthesized a family of sterol-modified glycerophospholipids (SML) in which the sn-1 or sn-2 position is covalently attached to cholesterol and the alternative position contains an aliphatic chain. The SML were used to explore how anchoring cholesterol to a phospholipid affects cholesterol behavior in a bilayer. Notably, cholesterol in the SML retains the membrane condensing properties of free cholesterol regardless of the chemistry or position of its attachment to the glycerol moiety of the phospholipid. SMLs by themselves formed liposomes upon hydration and in mixtures between an SML and diacylglycerophospholipids (C14 to C18 chain length) the thermotropic phase transition is eliminated at the SML equivalent of about 30 mol % free cholesterol. Osmotic-induced contents leakage from SML (C14-C18) liposomes depends upon the linkage and position of cholesterol but in general is similar to that observed in 3/2 diacylphosphatidylcholine/cholesterol (mole ratio) liposomes. SML liposomes are exceptionally resistant to contents release in the presence of serum at 37 degrees C. This is probably due to the fact that SML exchange between bilayers is more than 100 fold less than the exchange rate of free cholesterol in the same conditions. Importantly, SML liposomes containing doxorubicin are as effective in treating the murine C26 colon carcinoma as Doxil, a commercial liposome doxorubicin formulation. SMLs stabilize bilayers but do not exchange and hence provide a new tool for biophysical studies on membranes. They may improve liposomal drug delivery in organs predisposed to the extraction of free cholesterol from bilayers, such as the skin, lung, or blood.

  DOI：

  10.1021/ja8065557