sulphuretin 3'-O-β-glucopyranoside | 1360878-02-9

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 橙酮类黄酮
• 英文名称: sulphuretin 3'-O-β-glucopyranoside
• 英文别名: (2Z)-6-hydroxy-2-[[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methylidene]-1-benzofuran-3-one
• CAS: 1360878-02-9
• 化学式: C₂₁H₂₀O₁₀
• 分子量: 432.384
• InChiKey: PAEWWLDNEFSNIG-LTEMJKMTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  31
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  166
• 氢给体数：
  6
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  sulphuretin 3'-O-β-glucopyranoside 在 盐酸 作用下， 以 水 为溶剂， 反应 3.0h， 以0.8 mg的产率得到2-(3,4-二羟基苯亚甲基)-6-羟基-3(2H)-苯并呋喃酮
  参考文献：
  名称：

  Biflavonoids from Flowers of Butea monosperma (Lam.) Taub.

  摘要：

  A new aurone glucoside (1) and three new biflavonoids (12 - 14), together with fourteen known compounds, were isolated from the flowers of Butea monosperma (Lam.) Taub. The structures of the new compounds were established by ID, 2D NMR, MS and CD analyses. The isolated compounds were evaluated for their influenza A neuraminidase inhibitory activity and DPPH free-radical scavenging activity.

  DOI：

  10.3987/com-11-12275

文献信息

• Biflavonoids from Flowers of Butea monosperma (Lam.) Taub.
  作者：Yoshiki Kashiwada、Fakhruddin Ali Ahmed、Sang-Yong Kim、Shin-ichiro Kurimoto、Hisako Sasaki、Hirofumi Shibata、Yoshihisa Takaishi

  DOI：10.3987/com-11-12275

  日期：——

  A new aurone glucoside (1) and three new biflavonoids (12 - 14), together with fourteen known compounds, were isolated from the flowers of Butea monosperma (Lam.) Taub. The structures of the new compounds were established by ID, 2D NMR, MS and CD analyses. The isolated compounds were evaluated for their influenza A neuraminidase inhibitory activity and DPPH free-radical scavenging activity.