URB754
URB754 Basic information
- Product Name:
- URB754
- Synonyms:
-
- URB754
- 6-Methyl-2-[(4-methylphenyl)amino]-4H-3,1-benzoxazine-4-one
- 6-Methyl-2-[(4-methylphenyl)amino]-4H-3,1-benzoxazin-4-one
- 6-Methyl-2-(p-tolylMino)-4H-benzo[d][1,3]oxazin-4-one
- 6-Methyl-2-(p-tolylaMino)-1H-benzo[d][1,3]oxazin-4(2H)-one
- 6-Methyl-2-(p-tolylaMino)-4H-benzo[d][1,3]oxazin-4-one
- 6-Methyl-2-(p-tolylamino)-4H-3,1-benzoxazin-4-one
- URB754, >=98%
- CAS:
- 86672-58-4
- MF:
- C16H14N2O2
- MW:
- 266.3
- Product Categories:
-
- URB754 is a potent, noncompetitive inhibitor of MGL.
- Chemical for Research
- All Inhibitors
- Inhibitors
- Aromatics
- Heterocycles
- Research Chemical
- Mol File:
- 86672-58-4.mol
URB754 Chemical Properties
- Melting point:
- 238-240°C
- Boiling point:
- 434.0±48.0 °C(Predicted)
- Density
- 1.23±0.1 g/cm3(Predicted)
- storage temp.
- Refrigerator
- solubility
- DMSO (Slightly), Methanol (Slightly, Heated)
- pka
- 3.76±0.20(Predicted)
- form
- Off-white solid.
- color
- White to Off-White
URB754 Usage And Synthesis
Description
URB754 is a potent and noncompetitive inhibitor of monoacylglycerol lipase (MAGL), exhibiting an IC50 value of 200 nM for the recombinant rat brain enzyme. However, it does not inhibit human recombinant, rat brain, or mouse brain MAGL at concentrations up to 100 μM. There is evidence that the MAGL inhibitory activity of URB754 may be attributed to the impurity bis(methylthio)mercurane (IC50 = 11.9 nM for rat recombinant MAGL) that is found in commercial preparations. URB754 inhibits rat brain fatty acyl amide hydrolase (FAAH) with an IC50 value of 32 μM and binds weakly to the rat central cannabinoid (CB1) receptor with an IC50 value of 3.8 μM. It does not inhibit COX-1 or COX-2 at concentrations up to 100 μM. Inhibition of MAGL hydrolysis of 2-arachidonoyl glycerol (2-AG) is associated with enhanced stress-induced analgesia and may represent a novel drug target in pain and stress management.
Chemical Properties
Off-White Solid
Uses
URB754 is a potent, noncompetitive inhibitor of MGL, exhibiting an IC50 of 200 nM for the recombinant rat brain enzyme. It inhibits rat brain fatty acyl amide hydrolase (FAAH) less effectively with an IC50 of 32 μM and binds weakly to the rat CB1 receptor with an IC50 of 3.8 μM. It does not inhibit cyclooxygenase-1 (COX-1) or COX-2 at concentrations up to 100 μM. Inhibition of 2-AG hydrolysis is associated with enhanced stress-induced analgesia and may represent a novel drug target in pain and stress management.
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