作者
Bernd Kuhn,Martin Ritter,Benoit Hornsperger,Charles Bell,Buelent Koçer,Didier Rombach,Marius D. R. Lutz,Luca Gobbi,Martin Kuratli,Christian Bartelmus,Markus Bürkler,Raffael Koller,Paolo Tosatti,Iris Ruf,Melanie Guérard,Anto Pavlovic,Juliane Stephanus,Fionn O’Hara,Dennis Wetzl,Wiebke Saal,M. Stihle,Doris Roth,Melanie N. Hug,Sylwia Huber,Dominik Heer,Carsten Kroll,Andreas Topp,Manfred Schneider,Jürg Gertsch,Sandra Glasmacher,Mario van der Stelt,Andrea Martella,Matthias Wittwer,Ludovic Collin,Jörg Benz,Hans G. Richter,Uwe Grether
摘要
Monoacylglycerol lipase (MAGL) is a key enzyme involved in the metabolism of the endogenous signaling ligand 2-arachidonoylglycerol, a neuroprotective endocannabinoid intimately linked to central nervous system (CNS) disorders associated with neuroinflammation. In the quest for novel MAGL inhibitors, a focused screening approach on a Roche library subset provided a reversible benzoxazinone hit exhibiting high ligand efficiency. The subsequent design of the three-dimensional