N-(4'-hydroxy-3'-methoxybenzyl)docosa-(13Z)-enamide | 95548-17-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: N-(4'-hydroxy-3'-methoxybenzyl)docosa-(13Z)-enamide
• 英文别名: (Z)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-docos-13-enamide；13-Docosenamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-, (Z)-；(Z)-N-[(4-hydroxy-3-methoxyphenyl)methyl]docos-13-enamide
• CAS: 95548-17-7
• 化学式: C₃₀H₅₁NO₃
• 分子量: 473.74
• InChiKey: JHBDBWRBUIIWSE-KHPPLWFESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.3
• 重原子数：
  34
• 可旋转键数：
  22
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  58.6
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  芥酸 在 草酰氯 作用下， 以 乙醚 、 N,N-二甲基甲酰胺 为溶剂， 反应 3.0h， 生成 N-(4'-hydroxy-3'-methoxybenzyl)docosa-(13Z)-enamide
  参考文献：
  名称：

  香草。1.具有抗伤害感受和抗炎活性的辣椒素类似物。

  摘要：

  作为建立香草醛的结构活性关系的程序的一部分，辛辣成分辣椒素的类似物，母体结构的烷基链部分（以及衍生自高香草酸的相关化合物）发生了变化。在抗伤害感受和抗炎试验（大鼠和小鼠热板以及巴豆油刺激的小鼠耳朵）中，具有广泛变化的烷基链结构的化合物具有活性。短链化合物在上述测定中通过全身给药具有活性，但它们保留了辣椒素的高刺激性和急性毒性特征。相比之下，长链顺式不饱和物NE-19550（香草基油酰胺）和NE-28345（油基单香草酰胺）具有口服活性，刺激性较低，并且比辣椒素的急性毒性小。

  DOI：

  10.1021/jm00070a002

文献信息

• Elongation of the Hydrophobic Chain as a Molecular Switch: Discovery of Capsaicin Derivatives and Endogenous Lipids as Potent Transient Receptor Potential Vanilloid Channel 2 Antagonists
  作者：Aniello Schiano Moriello、Silvia López Chinarro、Olalla Novo Fernández、Jordi Eras、Pietro Amodeo、Ramon Canela-Garayoa、Rosa Maria Vitale、Vincenzo Di Marzo、Luciano De Petrocellis

  DOI：10.1021/acs.jmedchem.8b00734

  日期：2018.9.27

  potent pharmacological tools and endogenous modulators. Here we describe the discovery of novel synthetic long-chain capsaicin derivatives as potent TRPV2 antagonists in comparison to the totally inactive capsaicin, the role of their hydrophobic chain, and how the structure–activity relationships of such derivatives led, through a ligand-based approach, to the identification of endogenous long-chain

  瞬时受体电位香草2型（TRPV2）蛋白是非选择性Ca 2+由于缺乏可用的选择性和有效的药理学工具和内源性调节剂，TRPV亚家族的可渗透通道成员仍被认为是孤立的TRP通道。在这里，我们描述了通过完全基于配体的方法发现的新型合成长链辣椒素衍生物作为强效TRPV2拮抗剂（与完全无活性的辣椒素相比），它们的疏水链的作用以及这些衍生物的结构-活性关系如何导致的发现。 ，以鉴定充当TRPV2拮抗剂的内源性长链脂肪酸乙醇酰胺或伯酰胺。合成的和内源性的拮抗剂都表现出对以不同的动力学特征为特征的已知TRPV2激动剂的不同抑制作用。
• Compositions useful for producing analgesia
  申请人：THE PROCTER & GAMBLE COMPANY

  公开号：EP0132113A1

  公开（公告）日：1985-01-23

  A composition, useful for producing analgesia in humans or lower animals, comprising a safe and effective amount of: an Nf(substituted phenyl)methyl]-cis-monounsaturated alkenamide pharmaceutically-acceptable salts thereof, or mixtures thereof; and a pharmaceutically-acceptable carrier. Preferably, these alkenamides are N-vanillyl-cis-mono- unsaturated alkenamides. Methods of treatment, comprising administering a safe and effective amount of these alkenamides, pharmaceutically-acceptable salts thereof, or mixtures thereof, include methods of parenteral, oral, and topical administration.

  一种用于对人类或低等动物产生镇痛作用的组合物，包含安全有效量的：Nf（取代苯基）甲基]-顺式-单不饱和烯酰胺的药学上可接受的盐，或其混合物；以及药学上可接受的载体。这些烯酰胺最好是 N-香草醛-顺式-单不饱和烯酰胺。治疗方法包括施用安全有效量的这些烯酰胺、其药学上可接受的盐或其混合物，包括肠外、口服和局部给药方法。
• Evaluation of endogenous fatty acid amides and their synthetic analogues as potential anti-inflammatory leads
  作者：Hung The Dang、Gyeoung Jin Kang、Eun Sook Yoo、Jongki Hong、Jae Sue Choi、Hyung Sik Kim、Hae Young Chung、Jee H. Jung

  DOI：10.1016/j.bmc.2010.12.046

  日期：2011.2

  A series of endogenous fatty acid amides and their analogues (1-78) were prepared, and their inhibitory effects on pro-inflammatory mediators (NO, IL-1 beta, IL-6, and TNF-alpha) in LPS-activated RAW264.7 cells were evaluated. Their inhibitory activity on the pro-inflammatory chemokine MDC in IFN-gamma-activated HaCaT cells was also examined. The results showed that the activity is strongly dependent on the nature of the fatty acid part of the molecules. As expected, the amides derived from enone fatty acids showed significant activity and were more active than those derived from other types of fatty acids. A variation of the amine headgroup also altered bioactivity profile remarkably, possibly by modulating cell permeability. Regarding the amine part of the molecules, N-acyl dopamines exhibited the most potent activity (IC50 similar to 2 mu M). This is the first report of the inhibitory activity of endogenous fatty acid amides and their analogues on the production of nitric oxide, cytokines (IL-1 beta, IL-6, and TNF-alpha) and the chemokine MDC. This study suggests that the enone fatty acid-derived amides (such as N-acyl ethanolamines and N-acyl amino acids) and N-acyl dopamines may be potential anti-inflammatory leads. (C) 2010 Elsevier Ltd. All rights reserved.
• US4493848A
  申请人：——

  公开号：US4493848A

  公开（公告）日：1985-01-15
• US4564633A
  申请人：——

  公开号：US4564633A

  公开（公告）日：1986-01-14