(E)-3,6-Dioxo-docos-4-enoic acid methyl ester

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 酮酸及其衍生物
• 英文名称: (E)-3,6-Dioxo-docos-4-enoic acid methyl ester
• 英文别名: (E)-methyl-3,6-dioxo-4-docosenoate；methyl (E)-3,6-dioxodocos-4-enoate
• 化学式: C₂₃H₄₀O₄
• 分子量: 380.568
• InChiKey: OQTABBSTMSUYST-VHEBQXMUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.8
• 重原子数：
  27
• 可旋转键数：
  20
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  60.4
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  (5-hexadecylfuran-2-yl)acetic acid 在 水 、 溴 作用下， 以 丙酮 为溶剂， 生成 (E)-3,6-Dioxo-docos-4-enoic acid methyl ester
  参考文献：
  名称：

  Synthetic analogues of the manzamenones and plakoridines which inhibit DNA polymerase

  摘要：

  An array of novel analogues of the marine oxylipins, the manzamenones and plakoridines, have been prepared in divergent fashion using an approach modelled on a biogenetic theory. Many of the target compounds show potent inhibition of DNA polymerases alpha and beta and human terminal deoxynucleotidyl transferase (TdT).

  DOI：

  10.1016/j.bmcl.2006.03.005

文献信息

• Synthetic analogues of the manzamenones and plakoridines which inhibit DNA polymerase
  作者：Jeremy R. Doncaster、Laura L. Etchells、Neil M. Kershaw、Ryoichi Nakamura、Hazel Ryan、Ryo Takeuchi、Kengo Sakaguchi、Ali Sardarian、Roger C. Whitehead

  DOI：10.1016/j.bmcl.2006.03.005

  日期：2006.6

  An array of novel analogues of the marine oxylipins, the manzamenones and plakoridines, have been prepared in divergent fashion using an approach modelled on a biogenetic theory. Many of the target compounds show potent inhibition of DNA polymerases alpha and beta and human terminal deoxynucleotidyl transferase (TdT).