[(1R,2R,4S,5S,9R,10S,12S,13S,16R)-12-acetyloxy-2,16-dihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate | 1300655-67-7

• 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: [(1R,2R,4S,5S,9R,10S,12S,13S,16R)-12-acetyloxy-2,16-dihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate
• CAS: 1300655-67-7
• 化学式: C₂₄H₃₄O₇
• 分子量: 434.53
• InChiKey: YWMDJBRWUCLZAI-WERSQPBISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  31
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.79
• 拓扑面积：
  110
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  [(1R,2R,4S,5S,9R,10S,12S,13S,16R)-12-acetyloxy-2,16-dihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 在 三苯基膦 、 偶氮二甲酸二乙酯 、 对硝基苯甲酸 作用下， 以 四氢呋喃 为溶剂， 反应 1.0h， 以79%的产率得到[(3aR,5aS,6S,9aR,9bS,11S,11aR)-11-acetyloxy-6,9a-dimethyl-1-methylidene-2-oxo-3a,5,5a,7,8,9,9b,10,11,11a-decahydronaphtho[1,2-g][1]benzofuran-6-yl]methyl acetate
  参考文献：
  名称：

  Efficient transformation of 7,14-dihydroxy-ent-kaurenes to novel ent-abietanes having cis-fused α-methylene γ-lactones under Mitsunobu reaction conditions and their cytotoxicities

  摘要：

  Transformation of plant-origin 7,14-dihydroxy-ent-kaurenes to ent-abietanes having a cis-fused alpha-methylene gamma-lactones was accomplished efficiently under the Mitsunobu reaction conditions. The yields of the desired products were apparently influenced by the steric hindrance at C-1. The cytotoxic activity on P388 murine leukemia cells of the ent-abietanes having cis-fused alpha-methylene gamma-lactones produced were assayed. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2014.02.082
• 作为产物：
  描述：

  12O,18O-diacetylrabdokunmin C 7O,14O-acetonide 在 盐酸 作用下， 以 四氢呋喃 、 甲醇 、 水 为溶剂， 反应 24.0h， 以88%的产率得到[(1R,2R,4S,5S,9R,10S,12S,13S,16R)-12-acetyloxy-2,16-dihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate
  参考文献：
  名称：

  Efficient transformation of 7,14-dihydroxy-ent-kaurenes to novel ent-abietanes having cis-fused α-methylene γ-lactones under Mitsunobu reaction conditions and their cytotoxicities

  摘要：

  Transformation of plant-origin 7,14-dihydroxy-ent-kaurenes to ent-abietanes having a cis-fused alpha-methylene gamma-lactones was accomplished efficiently under the Mitsunobu reaction conditions. The yields of the desired products were apparently influenced by the steric hindrance at C-1. The cytotoxic activity on P388 murine leukemia cells of the ent-abietanes having cis-fused alpha-methylene gamma-lactones produced were assayed. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2014.02.082

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.
• Efficient transformation of 7,14-dihydroxy-ent-kaurenes to novel ent-abietanes having cis-fused α-methylene γ-lactones under Mitsunobu reaction conditions and their cytotoxicities
  作者：Yutaka Aoyagi、Kei Ozawa、Tatsuya Kobayashi、Tomoyo Hasuda、Ming-Yu Gui、Yong-Ri Jin、Xu-Wen Li、Haruhiko Fukaya、Reiko Yano、Yukio Hitotsuyanagi、Koichi Takeya

  DOI：10.1016/j.tet.2014.02.082

  日期：2014.5

  Transformation of plant-origin 7,14-dihydroxy-ent-kaurenes to ent-abietanes having a cis-fused alpha-methylene gamma-lactones was accomplished efficiently under the Mitsunobu reaction conditions. The yields of the desired products were apparently influenced by the steric hindrance at C-1. The cytotoxic activity on P388 murine leukemia cells of the ent-abietanes having cis-fused alpha-methylene gamma-lactones produced were assayed. (C) 2014 Elsevier Ltd. All rights reserved.