scorzoaustriacin 3-O-β-D-glucoside | 1210346-89-6

• 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: scorzoaustriacin 3-O-β-D-glucoside
• 英文别名: (3R,3aS,6aR,8S,9aR,9bS)-6,9-dimethylidene-3-[[(5-oxooxolan-2-yl)methylamino]methyl]-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one
• CAS: 1210346-89-6
• 化学式: C₂₆H₃₇NO₁₀
• 分子量: 523.58
• InChiKey: HMHFWUOWRNKNKO-DVIFFAQTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.6
• 重原子数：
  37
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  164
• 氢给体数：
  5
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  scorzoaustriacin 3-O-β-D-glucoside 在 三氟乙酸 作用下， 反应 5.0h， 以2 mg的产率得到1αH,5αH,6βH,7αH,11βH-3β-hydroxy-11α-[(tetrahydro-5-oxo-furan-2-yl)methylamino]methylguaia-4(15),10(14)-dien-12,6-olide
  参考文献：
  名称：

  Sesquiterpene Lactones from Scorzonera austriaca

  摘要：

  Six new sesquiterpene lactones, scorzoaustriacoside (1), scorzoaustriacin (2), scorzoaustriacin 3-O-beta-D-glucoside (3), 4-epi-dihydroestafiatol (4), 14-isovaleroxyscorzoaustricin (5). and 14-isovaleroxyscorzoaustricin sulfate (6), along with five known guaianolides, were isolated front all acetone extract of the roots of Scorzonera austriaca. The structures of the new compounds Were elucidated mainly by interpretation of their 1D and 2D NMR and FIRMS data. Several isolates obtained in this investigation were evaluated against a Small panel of cancer cell lines.

  DOI：

  10.1021/np900378c

文献信息

• Sesquiterpene Lactones from <i>Scorzonera austriaca</i>
  作者：Ying Zhu、Pei-Zhuo Hu、Zi-Wei He、Quan-Xiang Wu、Juan Li、Wang-Suo Wu

  DOI：10.1021/np900378c

  日期：2010.2.26

  Six new sesquiterpene lactones, scorzoaustriacoside (1), scorzoaustriacin (2), scorzoaustriacin 3-O-beta-D-glucoside (3), 4-epi-dihydroestafiatol (4), 14-isovaleroxyscorzoaustricin (5). and 14-isovaleroxyscorzoaustricin sulfate (6), along with five known guaianolides, were isolated front all acetone extract of the roots of Scorzonera austriaca. The structures of the new compounds Were elucidated mainly by interpretation of their 1D and 2D NMR and FIRMS data. Several isolates obtained in this investigation were evaluated against a Small panel of cancer cell lines.