单酰甘油脂肪酶
化学
丝氨酸水解酶
酶
丝氨酸
脂肪酶
体外
体内
生物化学
组合化学
内大麻素系统
受体
生物
生物技术
作者
Stefania Butini,Uwe Grether,Kwang‐Mook Jung,Alessia Ligresti,Marco Allarà,Annemarieke G. J. Postmus,Samuele Maramai,Simone Brogi,Alessandro Papa,Gabriele Carullo,David A. Sykes,Dmitry B. Veprintsev,Stefano Federico,Alessandro Grillo,Bruno Di Guglielmo,Anna Ramunno,Anna F. Stevens,Dominik Heer,Stefania Lamponi,Sandra Gemma
标识
DOI:10.1021/acs.jmedchem.3c01278
摘要
New potent, selective monoacylglycerol lipase (MAGL) inhibitors based on the azetidin-2-one scaffold ((±)-5a–v, (±)-6a–j, and (±)-7a–d) were developed as irreversible ligands, as demonstrated by enzymatic and crystallographic studies for (±)-5d, (±)-5l, and (±)-5r. X-ray analyses combined with extensive computational studies allowed us to clarify the binding mode of the compounds. 5v was identified as selective for MAGL when compared with other serine hydrolases. Solubility, in vitro metabolic stability, cytotoxicity, and absence of mutagenicity were determined for selected analogues. The most promising compounds ((±)-5c, (±)-5d, and (±)-5v) were used for in vivo studies in mice, showing a decrease in MAGL activity and increased 2-arachidonoyl-sn-glycerol levels in forebrain tissue. In particular, 5v is characterized by a high eudysmic ratio and (3R,4S)-5v is one of the most potent irreversible inhibitors of h/mMAGL identified thus far. These results suggest that the new MAGL inhibitors have therapeutic potential for different central and peripheral pathologies.
科研通智能强力驱动
Strongly Powered by AbleSci AI