feruloyl-6-O-β-D-glucopyranoside | 137887-25-3

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: feruloyl-6-O-β-D-glucopyranoside
• 英文别名: [(2R,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
• CAS: 137887-25-3
• 化学式: C₁₆H₂₀O₉
• 分子量: 356.329
• InChiKey: LVNFIOGAAUPIPC-YMILTQATSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.9
• 重原子数：
  25
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  146
• 氢给体数：
  5
• 氢受体数：
  9

安全信息

• 储存条件：
  储存温度应控制在2-8℃之间，需密封并保持干燥。

制备方法与用途

铁酰葡萄糖是一种具有抗氧化活性的天然产物[1][2]。

反应信息

• 作为产物：
  描述：

  3-(6-feruloyl-β-D-glucopyranosyl)rosmarinic acid 在 盐酸 作用下， 以 水 为溶剂， 反应 3.0h， 生成 feruloyl-6-O-β-D-glucopyranoside 、 TRANS-咖啡酸 、 丹参素
  参考文献：
  名称：

  Monoterpene glycosides, phenylpropanoids, and acacetin glycosides from Dracocephalum foetidum

  摘要：

  Chemical investigation of the acetone extract from the aerial parts of the Mongolian medicinal plant Dracocephalum foetidum resulted in the isolation of three limonene glycosides, a caffeic acid trimer, four rosmarinic acid glucosides, and five acacetin acyl glycosides, together with 13 known natural products. The chemical structures of all of the compounds were determined by spectroscopic analyses. Among these compounds three showed hyaluronidase inhibitory activity. In addition, one other compound showed stronger 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity than the positive control Trolox, whereas three other compounds demonstrated a similar activity to that of Trolox.

  DOI：

  10.1016/j.phytochem.2014.02.007

文献信息

• Monoterpene glycosides, phenylpropanoids, and acacetin glycosides from Dracocephalum foetidum
  作者：Erdenechimeg Selenge、Toshihiro Murata、Shiho Tanaka、Kenroh Sasaki、Javzan Batkhuu、Fumihiko Yoshizaki

  DOI：10.1016/j.phytochem.2014.02.007

  日期：2014.5

  Chemical investigation of the acetone extract from the aerial parts of the Mongolian medicinal plant Dracocephalum foetidum resulted in the isolation of three limonene glycosides, a caffeic acid trimer, four rosmarinic acid glucosides, and five acacetin acyl glycosides, together with 13 known natural products. The chemical structures of all of the compounds were determined by spectroscopic analyses. Among these compounds three showed hyaluronidase inhibitory activity. In addition, one other compound showed stronger 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity than the positive control Trolox, whereas three other compounds demonstrated a similar activity to that of Trolox.