1. Academic Validation
  2. URB602 inhibits monoacylglycerol lipase and selectively blocks 2-arachidonoylglycerol degradation in intact brain slices

URB602 inhibits monoacylglycerol lipase and selectively blocks 2-arachidonoylglycerol degradation in intact brain slices

  • Chem Biol. 2007 Dec;14(12):1357-65. doi: 10.1016/j.chembiol.2007.10.017.
Alvin R King 1 Andrea Duranti Andrea Tontini Silvia Rivara Anja Rosengarth Jason R Clapper Giuseppe Astarita Jennifer A Geaga Hartmut Luecke Marco Mor Giorgio Tarzia Daniele Piomelli
Affiliations

Affiliation

  • 1 Department of Pharmacology, University of California, Irvine, Irvine, CA 92697, USA.
Abstract

The N-aryl carbamate URB602 (biphenyl-3-ylcarbamic acid cyclohexyl ester) is an inhibitor of monoacylglycerol Lipase (MGL), a serine hydrolase involved in the biological deactivation of the endocannabinoid 2-arachidonoyl-sn-glycerol (2-AG). Here, we investigated the mechanism by which URB602 inhibits purified recombinant rat MGL by using a combination of biochemical and structure-activity relationship (SAR) approaches. We found that URB602 weakly inhibits recombinant MGL (IC(50) = 223 +/- 63 microM) through a rapid and noncompetitive mechanism. Dialysis experiments and SAR analyses suggest that URB602 acts through a partially reversible mechanism rather than by irreversible carbamoylation of MGL. Finally, URB602 (100 microM) elevates 2-AG levels in hippocampal slice cultures without affecting levels of other endocannabinoid-related substances. Thus, URB602 may provide a useful tool by which to investigate the physiological roles of 2-AG and explore the potential interest of MGL as a therapeutic target.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-100792
    99.51%, MGL Inhibitor