N-hexadecylcinnamamide

• 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: N-hexadecylcinnamamide
• 英文别名: N-hexadecyl-3-phenylprop-2-enamide
• 化学式: C₂₅H₄₁NO
• 分子量: 371.607
• InChiKey: ALWFJQMBWASSLV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.4
• 重原子数：
  27
• 可旋转键数：
  17
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  十六胺 、 肉桂酸 在 Candida antarctica lipase 作用下， 以79.8%的产率得到N-hexadecylcinnamamide
  参考文献：
  名称：

  Lipase-Catalyzed Solvent-Free Amidation of Phenolic Acids

  摘要：

  A series of N-alkyl-substituted amides, based on various phenolic acids, have been synthesized by the condensation of equimolar amounts of phenolic acids with different alkyl amines in the presence of Candida antarctica lipase at 60-90 degrees C in 16-20 h. The reactions were carried out in a solvent-free system without the use of any activating agents. All the products were obtained in appreciable amounts and the yields for different compounds varied between 75.6% and 83.5%. The synthesized compounds were characterized using spectroscopy techniques, namely infrared and NMR (H-1 and C-13).

  DOI：

  10.1080/00397911.2014.974611

文献信息

• Antileishmanial Activity of Cinnamic Acid Derivatives against Leishmania infantum
  作者：Mayara Castro de Morais、Gisele Alves Medeiros、Fernanda Silva Almeida、Juliana da Câmara Rocha、Yunierkis Perez-Castillo、Tatjana de Souza Lima Keesen、Damião Pergentino de Sousa

  DOI：10.3390/molecules28062844

  日期：——

  effects, which justify the efforts to find new antileishmanial drugs. Cinnamic acid derivatives have shown several pharmacological activities, including antiparasitic action. Therefore, in the present study, the biological evaluation of cinnamic acid and thirty-four derivatives against L. infantum is reported. The compounds were prepared by several synthesis methods and characterized by spectroscopic

  婴儿利什曼原虫是南美洲、地中海盆地以及西亚和中亚的内脏利什曼病 (VL) 的病原体。受影响最严重的国家巴西在 2017 年报告了 4297 例 VL 病例。L. infantum 由雌性白蛉在连续吸血期间传播。没有经过验证的疫苗可以预防感染，治疗依赖于经常出现严重副作用的药物，这证明了寻找新的抗利什曼病药物的努力是合理的。肉桂酸衍生物已显示多种药理活性，包括抗寄生虫作用。因此，在本研究中，报道了肉桂酸和 34 种衍生物对婴儿乳杆菌的生物学评价。这些化合物是通过几种合成方法制备的，并通过光谱技术和高分辨率质谱法进行了表征。结果表明，化合物 32（N-（4-异丙基苄基）肉桂酰胺）是最有效的抗利什曼病药物（IC50 = 33.71 μM），选择性指数最高（SI > 42.46），其次是化合物 15（胡椒基肉桂酸酯），IC50 = 42.80 μM 和 SI > 32.86。与两性霉素 B 相比，化合物
• Lipase-Catalyzed Solvent-Free Amidation of Phenolic Acids
  作者：Parshant Kaushik、Najam Akhtar Shakil、Jitendra Kumar、Braj Bhushan Singh

  DOI：10.1080/00397911.2014.974611

  日期：2015.3.4

  A series of N-alkyl-substituted amides, based on various phenolic acids, have been synthesized by the condensation of equimolar amounts of phenolic acids with different alkyl amines in the presence of Candida antarctica lipase at 60-90 degrees C in 16-20 h. The reactions were carried out in a solvent-free system without the use of any activating agents. All the products were obtained in appreciable amounts and the yields for different compounds varied between 75.6% and 83.5%. The synthesized compounds were characterized using spectroscopy techniques, namely infrared and NMR (H-1 and C-13).