(2R)-2-[(1S)-1,2-dihydroxyethyl]-4-heptadecoxy-3-phenylmethoxy-2H-furan-5-one | 98829-17-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氢呋喃
• 英文名称: (2R)-2-[(1S)-1,2-dihydroxyethyl]-4-heptadecoxy-3-phenylmethoxy-2H-furan-5-one
• CAS: 98829-17-5
• 化学式: C₃₀H₄₈O₆
• 分子量: 504.708
• InChiKey: PSKYLTNRFVMKND-RRPNLBNLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.58
• 重原子数：
  36.0
• 可旋转键数：
  22.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  85.22
• 氢给体数：
  2.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  (2R)-2-[(1S)-1,2-dihydroxyethyl]-4-heptadecoxy-3-phenylmethoxy-2H-furan-5-one 在 palladium on activated charcoal 氢气 作用下， 以 乙醇 为溶剂， 反应 18.0h， 生成 2-O-heptadecyl-L-ascorbic acid
  参考文献：
  名称：

  Studies on scavengers of active oxygen species. 1. Synthesis and biological activity of 2-O-alkylascorbic acids

  摘要：

  A novel series of 2-O-alkylascorbic acids (5a-u) was synthesized, and their scavenging activities against active oxygen species as well as their suppressive effects on the arrhythmias in rat heart ischemia-reperfusion models were evaluated. Some 2-O-alkylascorbic acids (5e-1) exhibited potent inhibiting activities against lipid peroxidation in rat brain homogenates and in alleviating effects in the ischemia-reperfusion models. Studies on the structure-activity relationship demonstrated that a free 3-enolic hydroxyl group and the longer alkyl chains substituted on the 2-hydroxyl group of ascorbic acid were beneficial for the biological and pharmacological activities. 2-O-Octadecylascorbic acid (5k, CV-3611), one of the most potent and promising compounds, markedly inhibited lipid peroxidation (IC50 = 4.3 X 10(-6) M) and alleviated myocardial lesions induced by ischemia-reperfusion at an oral dose of 1 mg/kg in rats.

  DOI：

  10.1021/jm00399a019
• 作为产物：
  描述：

  (2R)-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-4-heptadecoxy-3-phenylmethoxy-2H-furan-5-one 在 盐酸 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 6.0h， 生成 (2R)-2-[(1S)-1,2-dihydroxyethyl]-4-heptadecoxy-3-phenylmethoxy-2H-furan-5-one
  参考文献：
  名称：

  Studies on scavengers of active oxygen species. 1. Synthesis and biological activity of 2-O-alkylascorbic acids

  摘要：

  A novel series of 2-O-alkylascorbic acids (5a-u) was synthesized, and their scavenging activities against active oxygen species as well as their suppressive effects on the arrhythmias in rat heart ischemia-reperfusion models were evaluated. Some 2-O-alkylascorbic acids (5e-1) exhibited potent inhibiting activities against lipid peroxidation in rat brain homogenates and in alleviating effects in the ischemia-reperfusion models. Studies on the structure-activity relationship demonstrated that a free 3-enolic hydroxyl group and the longer alkyl chains substituted on the 2-hydroxyl group of ascorbic acid were beneficial for the biological and pharmacological activities. 2-O-Octadecylascorbic acid (5k, CV-3611), one of the most potent and promising compounds, markedly inhibited lipid peroxidation (IC50 = 4.3 X 10(-6) M) and alleviated myocardial lesions induced by ischemia-reperfusion at an oral dose of 1 mg/kg in rats.

  DOI：

  10.1021/jm00399a019