methyl 10-oxo-8-octadecenoate | 91363-63-2

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: methyl 10-oxo-8-octadecenoate
• 英文别名: methyl-(E)-10-oxooctadec-8-enoate；methyl 10-oxo-(E)-8-octadecenoate；methyl-10-oxooctadec-8-enoate；methyl (E)-10-oxooctadec-8-enoate
• CAS: 91363-63-2
• 化学式: C₁₉H₃₄O₃
• 分子量: 310.477
• InChiKey: LLJUIYYJBKXDIR-DTQAZKPQSA-N

物化性质

• 沸点：
  409.0±38.0 °C(Predicted)
• 密度：
  0.922±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6
• 重原子数：
  22
• 可旋转键数：
  16
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.79
• 拓扑面积：
  43.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  methyl 10-oxo-8-octadecenoate 在 palladium on activated charcoal 氢气 作用下， 以 甲醇 为溶剂， 生成 10-氧代十八烷酸甲酯
  参考文献：
  名称：

  Anti-inflammatory Constituents of the Red Alga Gracilaria verrucosa and Their Synthetic Analogues

  摘要：

  A chemical study on the anti-inflammatory components of the red alga Gracilaria verrucosa led to the isolation of new 11 -deoxyprostaglandins (1-4), a ceramide (5), and a C-16 keto fatty acid (6), along with known oxygenated fatty acids (7-14). Their structures were elucidated on the basis of NMR and MS data. The absolute configurations of compounds 1-5 were determined by Mosher's method. The anti-inflammatory activity of the isolated compounds (1-14) was evaluated by determining their inhibitory effects on the production of pro-inflammatory mediators (NO, IL-6, and TNF-alpha) in lipopolysaccharide (LPS)-activated RAW 264.7 murine macrophage cells. Compounds 9 and 10 exhibited the most potent activity. In the evaluation of these two compounds and derivatized analogues (15-40), the anti-inflammatory activity was enhanced in some synthetic analogues. These enone fatty acids were investigated as potential anti-inflammatory leads for the first time.

  DOI：

  10.1021/np070452q
• 作为产物：
  描述：

  methyl (E)-10-hydroperoxyoctadec-8-enoate 生成 methyl 10-oxo-8-octadecenoate
  参考文献：
  名称：

  CAPELLA, P.;CABONI, M. F.;BONAGA, G.;LERCKER, G., RIV. ITAL. SOSTANZE GRASSE, 65,(1988) N0, C. 629-631

  摘要：

  DOI：

文献信息

• Synthesis of 1-Palmitoyl-2-((E)-9- and (E)-10-nitrooleoyl)-sn-glycero-3-phosphatidylcholines
  作者：Alexander Lehr、Andrea Frank、Winfried Münch、Ulrich Dietz、Udo Nubbemeyer

  DOI：10.1055/s-0037-1611530

  日期：2019.9

  birthday Abstract Extensive investigation of nitrated phospholipids in connection with various biologically important processes requires reliable access to suitable material. A selective chemical synthesis introducing a defined nitrofatty acid at the sn-2 position of a 2-lyso sn-glycero-3-phosphatidylcholine was developed. Given that the nitroalkene moiety of both reactant nitrofatty acid derivative

  专用于汉斯-乌尔里希教授Reißig在他70之际个生日 抽象的 与各种生物学上重要的过程有关的硝化磷脂的广泛研究需要可靠地获得合适的材料。选择性化学合成引入在限定的nitrofatty酸SN -2的位置上的2-溶血SN开发了-甘油-3-磷脂酰胆碱。假定反应物硝基脂肪酸衍生物和产物酯的硝基烯烃部分均具有对亲核试剂加成的特别敏感性的特征，并且取决于中间体，随后的烯烃异构化和逆亨利型反应，引入了可靠的两步酯形成。与三氯苯甲酰氯反应后，硝基脂肪酸的活化成功，可以通过萃取后处理分离出混合的酸酐。随后与1-棕榈酰基-2-溶-sn-甘油-3-磷脂酰胆碱的反应使得通过使用最少的试剂可以高收率地实现sn -2酯化，避免了副产物的形成并促进了最终的分离和纯化。 与各种生物学上重要的过程有关的硝化磷脂的广泛研究需要可靠地获得合适的材料。选择性化学合成引入在限定的nitrofatty酸SN -2的位置上的2-溶血
• [EN] OXYLIPINS, PROCESSES FOR MAKING THE SAME, AND METHODS FOR USING THE SAME<br/>[FR] OXYLIPINES, LEURS PROCÉDÉS DE FABRICATION ET D'UTILISATION
  申请人：UNIV INDIANA TRUSTEES

  公开号：WO2022093755A1

  公开（公告）日：2022-05-05

  The present disclosure relates to oxylipins, processes for making the same, and methods of using. The process may form deuterated oxylipins that can be used as mass standards for mass spectroscopy.

  本公开涉及氧脂素、其制备过程和使用方法。该过程可以形成氘代氧脂素，可用作质谱分析的质量标准。
• A one-pot conversion of olefins to .alpha.,.beta.-unsaturated carbonyl compounds. An easy synthesis of 2-cyclopentenone and related compounds
  作者：Edward D. Mihelich、David J. Eickhoff

  DOI：10.1021/jo00170a060

  日期：1983.11
• MIHELICH, E. D.;EICKHOFF, D. J., J. ORG. CHEM., 1983, 48, N 22, 4135-4137
  作者：MIHELICH, E. D.、EICKHOFF, D. J.

  DOI：——

  日期：——
• Anti-inflammatory Constituents of the Red Alga <i>Gracilaria verrucosa</i> and Their Synthetic Analogues
  作者：Hung The Dang、Hye Ja Lee、Eun Sook Yoo、Pramod B. Shinde、Yoon Mi Lee、Jongki Hong、Dong Kyoo Kim、Jee H. Jung

  DOI：10.1021/np070452q

  日期：2008.2.1

  A chemical study on the anti-inflammatory components of the red alga Gracilaria verrucosa led to the isolation of new 11 -deoxyprostaglandins (1-4), a ceramide (5), and a C-16 keto fatty acid (6), along with known oxygenated fatty acids (7-14). Their structures were elucidated on the basis of NMR and MS data. The absolute configurations of compounds 1-5 were determined by Mosher's method. The anti-inflammatory activity of the isolated compounds (1-14) was evaluated by determining their inhibitory effects on the production of pro-inflammatory mediators (NO, IL-6, and TNF-alpha) in lipopolysaccharide (LPS)-activated RAW 264.7 murine macrophage cells. Compounds 9 and 10 exhibited the most potent activity. In the evaluation of these two compounds and derivatized analogues (15-40), the anti-inflammatory activity was enhanced in some synthetic analogues. These enone fatty acids were investigated as potential anti-inflammatory leads for the first time.