7α,10α,14β-10,14,18-trihydroxykaura-11,16-dien-15-one | 1300655-74-6

• 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: 7α,10α,14β-10,14,18-trihydroxykaura-11,16-dien-15-one
• 英文别名: (1R,2R,4S,5S,9R,10S,13S,16R)-2,16-dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadec-11-en-15-one
• CAS: 1300655-74-6
• 化学式: C₂₀H₂₈O₄
• 分子量: 332.44
• InChiKey: RSPLQGCXWSTZQC-YNDYFHGHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  24
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  77.8
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  12O,18O-diacetylrabdokunmin C 7O,14O-acetonide 在 盐酸 、 水 、 碳酸氢钠 、 三苯基膦 、 苯甲酸 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 40.33h， 生成 7α,10α,14β-10,14,18-trihydroxykaura-11,16-dien-15-one
  参考文献：
  名称：

  Synthesis of rabdokunmin C analogues and their inhibitory effect on NF-κB activation

  摘要：

  A series of rabdokunmin C analogues were prepared and their inhibitory effect on NF-kappa B activation was assayed. One of them, 18-acetyl-12-deoxy-11,12-dehydrorabdokunmin C (16) was found to be a promising candidate for an anti-inflammatory agent. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.02.002

文献信息

• Synthesis of rabdokunmin C analogues and their inhibitory effect on NF-κB activation
  作者：Yutaka Aoyagi、Yoshiyuki Adachi、Kei Ozawa、Chihiro Yokomizo、Ming-Yu Gui、Yong-Ri Jin、Xu-Wen Li、Naohito Ohno、Koichi Takeya

  DOI：10.1016/j.bmc.2011.02.002

  日期：2011.4

  A series of rabdokunmin C analogues were prepared and their inhibitory effect on NF-kappa B activation was assayed. One of them, 18-acetyl-12-deoxy-11,12-dehydrorabdokunmin C (16) was found to be a promising candidate for an anti-inflammatory agent. (C) 2011 Elsevier Ltd. All rights reserved.