内大麻素系统
单酰甘油脂肪酶
大麻素受体
化学
大麻素
酶
立体化学
组合化学
受体
生物化学
敌手
作者
Spyros P. Nikas,Lipin Ji,Yingpeng Liu,Markos‐Orestis Georgiadis,Amey Dopeshwarkar,Alex Straiker,Shalley N. Kudalkar,Anastasiia Sadybekov,Michaela Dvořáková,Vsevolod Katritch,Ken Mackie,Lawrence J. Marnett,Alexandros Makriyannis
标识
DOI:10.1021/acsmedchemlett.4c00175
摘要
2-Arachidonoyl glycerol (2-AG) is the principal endogenously produced ligand for the cannabinoid CB1 and CB2 receptors (CBRs). The lack of potent and efficacious 2-AG ligands with resistance against metabolizing enzymes represents a significant void in the armamentarium of research tools available for studying eCB system molecular constituents and their function. Herein we report the first endocannabinoid glyceride templates with remarkably high potency and efficacy at CBRs. Two of our lead chiral 2-AG analogs, namely, (13S)- and (13R)-Me-2-AGs, potently inhibit excitatory neurotransmission via CB1 while they are endowed with excellent resistance to the oxidizing enzyme COX-2. Our SAR results are supported by docking studies of the key analog and 2-AG on the crystal structures of CB1.
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