Nikas Spyros P, Ji Lipin, Liu Yingpeng, Georgiadis Markos-Orestis, Dopeshwarkar Amey, Straiker Alex, Kudalkar Shalley, Sadybekov Anastasiia V, Dvorakova Michaela, Katritch Vsevolod, Mackie Ken, Marnett Lawrence, Makriyannis Alexandros
Center for Drug Discovery and Department of Pharmaceutical Sciences, Northeastern University, Boston, Massachusetts 02115, United States.
Department of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, Indiana 47405, United States.
ACS Med Chem Lett. 2024 May 28;15(6):965-971. doi: 10.1021/acsmedchemlett.4c00175. eCollection 2024 Jun 13.
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, (13)- and (13)-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.
2-花生四烯酸甘油酯(2-AG)是内源性产生的主要大麻素CB1和CB2受体(CBRs)配体。缺乏对代谢酶具有抗性的强效且有效的2-AG配体,是可用于研究内源性大麻素系统分子成分及其功能的研究工具库中的一个重大空白。在此,我们报道了首个在内源性大麻素甘油酯模板方面,对CBRs具有显著高效力和功效的研究成果。我们的两个主要手性2-AG类似物,即(13)-和(13)-甲基-2-AGs,通过CB1有效抑制兴奋性神经传递,同时它们对氧化酶COX-2具有优异的抗性。我们的构效关系(SAR)结果得到了关键类似物和2-AG在CB1晶体结构上对接研究的支持。