作者:Fen-Mei Yao、Sonya L. Palmer、Atmaram D. Khanolkar、Xiaoyu Tian、Jianxin Guo、Alexandros Makriyannis
DOI:10.1002/jlcr.650
日期:2003.2
Four isotopically labeled, metabolically stable analogs of arachidony-lethanolamide (anandamide), an endogenous cannabinoid ligand, were synthesized via a five-step reaction sequence starting from arachidonic acid. These stable methanandamide derivatives will serve as probes for studying the conformational properties of anandamide in model membrane systems using solid-state NMR spectroscopy. The synthetic methods described can be applied to the preparations of other anandamide analogs with isotopic labeling in different positions of the molecule, which could be utilized in biochemical and pharmacological experiments. Copyright © 2002 John Wiley & Sons, Ltd.
四种同位素标记的代谢稳定的花生四烯酸乙醇酰胺(内源性大麻素配体,anandamide)类物质通过从花生四烯酸开始的五步反应序列合成。这些稳定的甲基安索胺衍生物将作为探针,用于研究在模型膜系统中安索胺的构象特性,采用固态NMR光谱法。所描述的合成方法可以应用于其他带有不同位置同位素标记的安索胺类物质的制备,这些物质可用于生化和药理实验。版权 © 2002 John Wiley & Sons, Ltd.