notoginsenoside SFt₃ | 1351360-27-4

• 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: notoginsenoside SFt₃
• 英文别名: 3β,12β-dihydroxydammer-20(21),24-diene-3-O-[β-D-xylopyranosyl-(1->2)-O-β-D-glucopyranosyl-(1->2)-O-β-D-glucopyranoside]；centelloside A；(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,5-dien-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
• CAS: 1351360-27-4
• 化学式: C₄₇H₇₈O₁₆
• 分子量: 899.127
• InChiKey: VYXLDGRUZLUGFS-WLAAAXFUSA-N

物化性质

• 沸点：
  968.8±65.0 °C(Predicted)
• 密度：
  1.34±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  63
• 可旋转键数：
  12
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  258
• 氢给体数：
  10
• 氢受体数：
  16

反应信息

• 作为反应物：
  描述：

  notoginsenoside SFt₃ 在 盐酸 作用下， 以 水 为溶剂， 反应 3.0h， 生成 D-来苏糖 、 葡萄糖
  参考文献：
  名称：

  Two new dammarane monodesmosides fromCentella asiatica

  摘要：

  Two new dammarane monodesmosides centellosides A (1) and B (2), and two new natural products ginsenosides Mc (10) and Y (11), together with 11 known compounds (3-9 and 12-15) reported for the first time from this genus, were isolated from the whole plants of Centella asiatica. All structures were elucidated by spectroscopic techniques and chemical methods, and compared with literature values. All the isolated compounds were evaluated in vitro for cytotoxicity.

  DOI：

  10.1080/10286020.2011.588212

文献信息

• Two new dammarane monodesmosides from<i>Centella asiatica</i>
  作者：Xiao-Xiang Weng、Yan Shao、Yun-Yan Chen、Wen Gao、Liang Cheng、De-Yun Kong

  DOI：10.1080/10286020.2011.588212

  日期：2011.8

  Two new dammarane monodesmosides centellosides A (1) and B (2), and two new natural products ginsenosides Mc (10) and Y (11), together with 11 known compounds (3-9 and 12-15) reported for the first time from this genus, were isolated from the whole plants of Centella asiatica. All structures were elucidated by spectroscopic techniques and chemical methods, and compared with literature values. All the isolated compounds were evaluated in vitro for cytotoxicity.