lauryl p-coumarate | 1173709-57-3

• 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: lauryl p-coumarate
• 英文别名: Dodecyl p-coumarate；dodecyl (E)-3-(4-hydroxyphenyl)prop-2-enoate
• CAS: 1173709-57-3
• 化学式: C₂₁H₃₂O₃
• 分子量: 332.483
• InChiKey: IUQAFQCPIPHTKY-SAPNQHFASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.4
• 重原子数：
  24
• 可旋转键数：
  14
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  十二烷醇 在 吡啶 、 苯胺 作用下， 以 环己烷 、 甲苯 为溶剂， 反应 4.0h， 生成 lauryl p-coumarate
  参考文献：
  名称：

  Discovery of neurotrophic agents based on hydroxycinnamic acid scaffold

  摘要：

  The number of people affected by neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease is rapidly increasing owing to the global increase in life expectancy. Small molecules with neurotrophic effects have great potential for management of these neurological disorders. In this study, different (C1–C12) alkyl ester derivatives of hydroxycinnamic acids (HCAs) were synthesized (a total of 30 compounds). The neurotrophic capacity of the test compounds was examined by measuring promotion of survival in serum‐deprived conditions and enhancement of nerve growth factor (NGF)‐induced neurite outgrowth in PC12 neuronal cells. p‐Coumaric, ferulic, and sinapic acids and their esters did not alter cell survival, while caffeic acid and all its alkyl esters, especially decyl and dodecyl caffeate, significantly promoted neuronal survival at 25 μm. Methyl, ethyl, propyl, and butyl caffeate esters also significantly enhanced NGF‐induced neurite outgrowth, among which the most effective ones were propyl and butyl esters, which at 5 μm led to 25‐ and 22‐fold increases in the number of neurites, respectively. The findings of the docking study suggested phosphatidylinositol 3‐kinase (PI3K) as the potential molecular target. In conclusion, our findings demonstrate that alkyl esters of caffeic acid can be useful as scaffolds for the discovery of therapeutic agents for neurodegenerative diseases.

  DOI：

  10.1111/cbdd.12829

文献信息

• Synthesis and DNA Polymerase .ALPHA. and .BETA. Inhibitory Activity of Alkyl p-Coumarates and Related Compounds
  作者：Katsumi Nishimura、Yukiko Takenaka、Manami Kishi、Takao Tanahashi、Hiromi Yoshida、Chiaki Okuda、Yoshiyuki Mizushina

  DOI：10.1248/cpb.57.476

  日期：——

  trans- and cis-Icosyl, docosyl, and tetracosyl p-coumarates, constituents of Artemisia annua L., and their structurally-related compounds were synthesized and evaluated for inhibitory activity on DNA polymerases alpha and beta. Among 30 compounds synthesized, octadecyl trans- and cis-p-coumarates and octadecyl p-hydroxyphenylpropiolate showed strong inhibitory activity on DNA polymerases alpha and

  合成了Artemisia annua L.的组成部分的反式和顺式-二十烷基，二十二烷基和十四烷基对-香豆酸酯及其结构相关的化合物，并评估了它们对DNA聚合酶α和β的抑制活性。在合成的30种化合物中，十八烷基反式和顺式对-香豆酸酯和十八烷基对羟基苯丙酸酯显示出对DNA聚合酶α和β的强抑制活性。
• Alkyl and Aryl Derivatives Based on p-Coumaric Acid Modification and Inhibitory Action against Leishmania braziliensis and Plasmodium falciparum
  作者：Susiany P. Lopes、Lina M. Yepes、Yunierkis Pérez-Castillo、Sara M. Robledo、Damião P. de Sousa

  DOI：10.3390/molecules25143178

  日期：——

  worldwide and are creating a public health problem. The present work evaluates the leishmanicidal and antiplasmodial action of a series of twelve p-coumaric acid derivatives. Of the tested derivatives, eight presented antiparasitic activities 1–3, 8–12. The hexyl p-coumarate derivative (9) (4.14 ± 0.55 μg/mL; selectivity index (SI) = 2.72) showed the highest leishmanicidal potency against the Leishmania

  在低收入人群中，被忽视的疾病是导致死亡的主要原因。其中，利什曼病和疟疾是寄生虫、原生动物感染，影响着全世界数百万人，并正在造成公共卫生问题。目前的工作评估了一系列十二种对香豆酸衍生物的杀利什曼原虫和抗疟原虫的作用。在测试的衍生物中，八种具有抗寄生虫活性 1-3、8-12。对香豆酸己酯衍生物 (9) (4.14 ± 0.55 μg/mL；选择性指数 (SI) = 2.72) 显示出对巴西利什曼原虫无鞭毛体形式的最高利什曼原虫杀灭效力。分子对接研究结果表明，该化合物抑制醛脱氢酶 (ALDH)、丝裂原活化激酶蛋白 (MPK4) 和 DNA 拓扑异构酶 2 (TOP2)，所有这些都是巴西利什曼原虫发育的关键酶。数据表明，这些酶通过范德华键、疏水相互作用和氢键与同一化合物的酚类和脂肪族部分相互作用。在分析的其他化合物中，对香豆酸甲酯 (64.59 ± 2.89 μg/mL；IS = 0.1) 显示出
• 一种对香豆酸酯及其合成方法与应用
  申请人：华南理工大学

  公开号：CN113402392B

  公开（公告）日：2023-04-28
• Discovery of neurotrophic agents based on hydroxycinnamic acid scaffold
  作者：Razieh Hosseini、Fatemeh Moosavi、Hamid Rajaian、Tiago Silva、Diogo Magalhães e Silva、Pedro Soares、Luciano Saso、Najmeh Edraki、Ramin Miri、Fernanda Borges、Omidreza Firuzi

  DOI：10.1111/cbdd.12829

  日期：2016.12

  The number of people affected by neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease is rapidly increasing owing to the global increase in life expectancy. Small molecules with neurotrophic effects have great potential for management of these neurological disorders. In this study, different (C1–C12) alkyl ester derivatives of hydroxycinnamic acids (HCAs) were synthesized (a total of 30 compounds). The neurotrophic capacity of the test compounds was examined by measuring promotion of survival in serum‐deprived conditions and enhancement of nerve growth factor (NGF)‐induced neurite outgrowth in PC12 neuronal cells. p‐Coumaric, ferulic, and sinapic acids and their esters did not alter cell survival, while caffeic acid and all its alkyl esters, especially decyl and dodecyl caffeate, significantly promoted neuronal survival at 25 μm. Methyl, ethyl, propyl, and butyl caffeate esters also significantly enhanced NGF‐induced neurite outgrowth, among which the most effective ones were propyl and butyl esters, which at 5 μm led to 25‐ and 22‐fold increases in the number of neurites, respectively. The findings of the docking study suggested phosphatidylinositol 3‐kinase (PI3K) as the potential molecular target. In conclusion, our findings demonstrate that alkyl esters of caffeic acid can be useful as scaffolds for the discovery of therapeutic agents for neurodegenerative diseases.