两种新型甲基取代花生四烯酸衍生物以对映选择性方式从市售手性结构单元制备,并被发现是开发 (13 S )-甲基取代花生四烯酸类似物的极好模板。合成的化合物之一,即(13 S ,5 Z ,8 Z ,11 Z ,14 Z )-13-甲基-二十碳-5,8,11,14-四烯酸N- (2-羟乙基)酰胺,是一种内源性大麻素类似物,对 CB1 大麻素受体具有非常高的亲和力。
Design and Synthesis of (13S)-Methyl-Substituted Arachidonic Acid Analogues: Templates for Novel Endocannabinoids
作者:Demetris P. Papahatjis、Victoria R. Nahmias、Spyros P. Nikas、Marion Schimpgen、Alexandros Makriyannis
DOI:10.1002/chem.200902880
日期:2010.4.6
Two novel methyl‐substituted arachidonicacid derivatives were prepared in an enantioselective manner from commercially available chiral building blocks, and were found to be excellent templates for the development of (13S)‐methyl‐substituted anandamide analogues. One of the compounds synthesized, namely, (13S,5Z,8Z,11Z,14Z)‐13‐methyl‐eicosa‐5,8,11,14‐tetraenoic acid N‐(2‐hydroxyethyl)amide, is an
两种新型甲基取代花生四烯酸衍生物以对映选择性方式从市售手性结构单元制备,并被发现是开发 (13 S )-甲基取代花生四烯酸类似物的极好模板。合成的化合物之一,即(13 S ,5 Z ,8 Z ,11 Z ,14 Z )-13-甲基-二十碳-5,8,11,14-四烯酸N- (2-羟乙基)酰胺,是一种内源性大麻素类似物,对 CB1 大麻素受体具有非常高的亲和力。