[2-(4-methoxyanilino)-2-oxoethyl] (E)-3-[4-[(3,4-dichlorophenyl)methoxy]-3,5-dimethoxyphenyl]prop-2-enoate | 1048005-10-2

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: [2-(4-methoxyanilino)-2-oxoethyl] (E)-3-[4-[(3,4-dichlorophenyl)methoxy]-3,5-dimethoxyphenyl]prop-2-enoate
• CAS: 1048005-10-2
• 化学式: C₂₇H₂₅Cl₂NO₇
• 分子量: 546.404
• InChiKey: ZRUNQOKSKCDITE-VZUCSPMQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  37
• 可旋转键数：
  12
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  92.3
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  4-O-(3,4-dichlorobenzyl)sinapic acid ethyl ester 、 2-氯-N-(4-甲氧基苯基)-乙酰胺 在 potassium iodide 、 potassium hydroxide 作用下， 以 N,N-二甲基甲酰胺 、 乙醇 、 水 为溶剂， 反应 0.33h， 以72%的产率得到[2-(4-methoxyanilino)-2-oxoethyl] (E)-3-[4-[(3,4-dichlorophenyl)methoxy]-3,5-dimethoxyphenyl]prop-2-enoate
  参考文献：
  名称：

  Synthesis, biological evaluation, and structure–activity relationship study of novel cytotoxic aza-caffeic acid derivatives

  摘要：

  Three series of aza-caffeic acid derivatives with different linkers were designed and synthesized. Each of the synthesized derivatives was then used in cytotoxicity screening on either 8 or 12 human cancer cell lines. The structure-activity relationships on three structural regions A, B, and C are analyzed in detail, indicating that a nine bond linker B, containing a piperazine unit, is the most favorable linker leading to the generation of molecules with potent cytotoxicities. Compound (E)-1-(4-(3,4-dichlorobenzyl) piperazin-1-yl)-3-(4-(4-ethoxybenzyloxy)-3,5-dimethoxyphenyl) prop-2-en-1-one (80) exhibited the most significant and selective cytotoxicity to KB, BEL7404, K562, and Eca109 cell lines, with IC(50) values of 0.2, 2.0, 1.7, and 1.1 mu M, respectively, stronger than that seen for caffeic acid phenethyl ester (CAPE) and cisplatin (CDDP). Flow cytometric and western blot analysis indicate that compound 80 plays a role in mitochondria-dependent apoptosis activity by suppressing K562 cell proliferation in a concentration- and time-dependent manner. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.07.016