URB754 Has No Effect on the Hydrolysis or Signaling Capacity of 2-AG in the Rat Brain

This publication has 15 references indexed in Scilit:

• Fatty Acid Amide Hydrolase Inhibitors from Virtual Screening of the Endocannabinoid System
  Journal of Medicinal Chemistry, 2006
• The basic secretagogue compound 48/80 activates G proteins indirectlyviastimulation of phospholipase D–lysophosphatidic acid receptor axis and 5‐HT_1Areceptors in rat brain sections
  British Journal of Pharmacology, 2006
• Selective inhibition of 2-AG hydrolysis enhances endocannabinoid signaling in hippocampus
  Nature Neuroscience, 2005
• Characterization of the Sulfhydryl-Sensitive Site in the Enzyme Responsible for Hydrolysis of 2- Arachidonoyl-Glycerol in Rat Cerebellar Membranes
  Chemistry & Biology, 2005
• RNA Interference Suggests a Primary Role for Monoacylglycerol Lipase in the Degradation of the Endocannabinoid 2-Arachidonoylglycerol
  Molecular Pharmacology, 2004
• Segregation of two endocannabinoid‐hydrolyzing enzymes into pre‐ and postsynaptic compartments in the rat hippocampus, cerebellum and amygdala
  European Journal of Neuroscience, 2004
• Monoglyceride lipase-like enzymatic activity is responsible for hydrolysis of 2-arachidonoylglycerol in rat cerebellar membranes
  Biochemical Pharmacology, 2004
• Despite substantial degradation, 2‐arachidonoylglycerol is a potent full efficacy agonist mediating CB₁ receptor‐dependent G‐protein activation in rat cerebellar membranes
  British Journal of Pharmacology, 2001
• cDNA Cloning, Tissue Distribution, and Identification of the Catalytic Triad of Monoglyceride Lipase
  Journal of Biological Chemistry, 1997
• Synthesis of 3-Aryl-2,4-dioxo-1,2,3,4-tetrahydroquinazolines and 2-Arylamino-4-oxo-4H-3,1-benzoxazines from MethylN-Aryldithiocarbamates
  Synthesis, 1983