methyl ((4aR,4bS,6aR,7R,10aR,10bR,12R,12aR)-13-isopropyl-7,10a-dimethyl-1,4-dioxo-2,3,4,4a,5,6,6a,7,8,9,10,10a,10b,11,12,12a-hexadecahydro-1H-4b,12-ethenochrysene-7-carbonyl)-L-valinate | 1192804-25-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: methyl ((4aR,4bS,6aR,7R,10aR,10bR,12R,12aR)-13-isopropyl-7,10a-dimethyl-1,4-dioxo-2,3,4,4a,5,6,6a,7,8,9,10,10a,10b,11,12,12a-hexadecahydro-1H-4b,12-ethenochrysene-7-carbonyl)-L-valinate
• CAS: 1192804-25-3
• 化学式: C₃₂H₄₇NO₅
• 分子量: 525.729
• InChiKey: ZRRICRVDRTWWDE-JESZCFMTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.29
• 重原子数：
  38.0
• 可旋转键数：
  5.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.81
• 拓扑面积：
  89.54
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  methyl ((4aR,4bS,6aR,7R,10aR,10bR,12R,12aR)-13-isopropyl-7,10a-dimethyl-1,4-dioxo-2,3,4,4a,5,6,6a,7,8,9,10,10a,10b,11,12,12a-hexadecahydro-1H-4b,12-ethenochrysene-7-carbonyl)-L-valinate 在 水 、 sodium hydroxide 作用下， 以 甲醇 为溶剂， 反应 4.0h， 以87%的产率得到
  参考文献：
  名称：

  Synthesis of dihydroquinopimaric acid conjugates with amino acids

  摘要：

  Synthesis of dihydroquinopimaric acid amides and their 2 beta-succinyl and 2 beta-phthalyl derivatives containing residues of amino acids was carried out for the first time. Antiviral properties of the compounds synthesized were investigated.

  DOI：

  10.1134/s1068162009030157
• 作为产物：
  描述：

  dihydroquinopimaric acid chloride 、 L-缬氨酸甲酯盐酸盐 在 三乙胺 作用下， 以 氯仿 为溶剂， 反应 2.0h， 以59%的产率得到methyl ((4aR,4bS,6aR,7R,10aR,10bR,12R,12aR)-13-isopropyl-7,10a-dimethyl-1,4-dioxo-2,3,4,4a,5,6,6a,7,8,9,10,10a,10b,11,12,12a-hexadecahydro-1H-4b,12-ethenochrysene-7-carbonyl)-L-valinate
  参考文献：
  名称：

  Synthesis of dihydroquinopimaric acid conjugates with amino acids

  摘要：

  Synthesis of dihydroquinopimaric acid amides and their 2 beta-succinyl and 2 beta-phthalyl derivatives containing residues of amino acids was carried out for the first time. Antiviral properties of the compounds synthesized were investigated.

  DOI：

  10.1134/s1068162009030157