(E)-N-(6-((3,5-dimethyladamantan-1-yl)amino)hexyl)-3-(4-hydroxy-3-methoxyphenyl)acrylamide

• 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: (E)-N-(6-((3,5-dimethyladamantan-1-yl)amino)hexyl)-3-(4-hydroxy-3-methoxyphenyl)acrylamide
• 英文别名: (E)-N-[6-[(3,5-dimethyl-1-adamantyl)amino]hexyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide
• 化学式: C₂₈H₄₂N₂O₃
• 分子量: 454.653
• InChiKey: RBRMEBJXSQTZBH-PKNBQFBNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  33
• 可旋转键数：
  11
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.68
• 拓扑面积：
  70.6
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  盐酸美金刚 在 盐酸 、 potassium carbonate 、 1-羟基苯并三唑 、 1,2-二氯乙烷 、 potassium iodide 作用下， 以 1,4-二氧六环 、 N,N-二甲基甲酰胺 为溶剂， 20.0 ℃ 、1.72 MPa 条件下， 反应 1.17h， 生成 (E)-N-(6-((3,5-dimethyladamantan-1-yl)amino)hexyl)-3-(4-hydroxy-3-methoxyphenyl)acrylamide
  参考文献：
  名称：

  Merging memantine and ferulic acid to probe connections between NMDA receptors, oxidative stress and amyloid-β peptide in Alzheimer's disease

  摘要：

  N-methyl-D-aspartate receptors (NMDAR) are critically involved in the pathogenesis of Alzheimer's disease (AD). Acting as an open-channel blocker, the anti-AD drug memantine preferentially targets NMDAR overactivation, which has been proposed to trigger neurotoxic events mediated by amyloid beta peptide (A beta) and oxidative stress. In this study, we applied a multifunctional approach by conjugating memantine to ferulic acid, which is known to protect the brain from A beta neurotoxicity and neuronal death caused by ROS. The most interesting compound (7) behaved, like memantine, as a voltage-dependent antagonist of NMDAR (IC50 = 6.9 mu M). In addition, at 10 mu M concentration, 7 exerted antioxidant properties both directly and indirectly through the activation of the Nrf-2 pathway in SH-SY5Y cells. At the same concentration, differently from the parent compounds memantine and ferulic acid alone, it was able to modulate A beta production, as revealed by the observed increase of the non-amyloidogenic sAPP alpha in H4-SW cells. These findings suggest that compound 7 may represent a promising tool for investigating NMDAR-mediated neurotoxic events involving A beta burden and oxidative damage. (C) 2019 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2019.07.011