3β-[2-(morpholine-4-yl)acetyloxy]olean-12-en-28-oic acid | 1428655-84-8

• 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: 3β-[2-(morpholine-4-yl)acetyloxy]olean-12-en-28-oic acid
• 英文别名: (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-(2-morpholin-4-ylacetyl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
• CAS: 1428655-84-8
• 化学式: C₃₆H₅₇NO₅
• 分子量: 583.852
• InChiKey: NCVDRBVPFMKWFX-IGXJBCQUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.5
• 重原子数：
  42
• 可旋转键数：
  5
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.89
• 拓扑面积：
  76.1
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  benzyl 3β-(2-chloroacetyloxy)olean-12-en-28-oate 在 palladium 10% on activated carbon 、 氢气 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 14.0h， 生成 3β-[2-(morpholine-4-yl)acetyloxy]olean-12-en-28-oic acid
  参考文献：
  名称：

  Synthesis and cytotoxicity evaluation of oleanolic acid derivatives

  摘要：

  Twelve derivatives of oleanolic acid (1) have been synthesized and evaluated for their inhibitory activities against the growth of prostate PC3, breast MCF-7, lung A549, and gastric BGC-823 cancer cells by MU assays. Within these series of derivatives, compound 17 exhibited the most potent cytotoxicity against PC3 cell line (IC50 = 0.39 mu M) and compound 28 displayed the best activity against A549 cell line (IC50 = 0.22 mu M). SAR analysis indicates that H-donor substitution at C-3 position of oleanolic acid may be advantageous for improvement of cytotoxicity against PC3, A549 and MCF-7 cell lines. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.01.129

文献信息

• Synthesis and cytotoxicity evaluation of oleanolic acid derivatives
  作者：Jia Hao、Jun Liu、Xiaoan Wen、Hongbin Sun

  DOI：10.1016/j.bmcl.2013.01.129

  日期：2013.4

  Twelve derivatives of oleanolic acid (1) have been synthesized and evaluated for their inhibitory activities against the growth of prostate PC3, breast MCF-7, lung A549, and gastric BGC-823 cancer cells by MU assays. Within these series of derivatives, compound 17 exhibited the most potent cytotoxicity against PC3 cell line (IC50 = 0.39 mu M) and compound 28 displayed the best activity against A549 cell line (IC50 = 0.22 mu M). SAR analysis indicates that H-donor substitution at C-3 position of oleanolic acid may be advantageous for improvement of cytotoxicity against PC3, A549 and MCF-7 cell lines. (C) 2013 Elsevier Ltd. All rights reserved.