Design and Synthesis of Novel Spiro Derivatives as Potent and Reversible Monoacylglycerol Lipase (MAGL) Inhibitors: Bioisosteric Transformation from 3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl Moiety.
J Med Chem
; 64(15): 11014-11044, 2021 08 12.
Article
in En
| MEDLINE
| ID: mdl-34328319
Full text:
1
Database:
MEDLINE
Main subject:
Oxazines
/
Spiro Compounds
/
Drug Design
/
Enzyme Inhibitors
/
Monoacylglycerol Lipases
Limits:
Humans
Language:
En
Year:
2021
Type:
Article