CAS 86672-58-4
:URB 754
Description:
URB 754, with the CAS number 86672-58-4, is a chemical compound known for its role as a selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH). This enzyme is responsible for the breakdown of endocannabinoids, which are naturally occurring compounds in the body that interact with cannabinoid receptors. By inhibiting FAAH, URB 754 increases the levels of endocannabinoids, potentially enhancing their effects on pain, mood, and other physiological processes. The compound is often studied in the context of neuropharmacology and has been investigated for its potential therapeutic applications in conditions such as anxiety, depression, and pain management. URB 754 is characterized by its specific binding affinity to FAAH, which distinguishes it from other compounds that may affect the endocannabinoid system. Its chemical structure includes functional groups that contribute to its biological activity, making it a subject of interest in medicinal chemistry and drug development. However, as with any pharmacological agent, further research is necessary to fully understand its efficacy and safety profile in clinical settings.
Formula:C16H14N2O2
InChI:InChI=1/C16H14N2O2/c1-10-3-6-12(7-4-10)17-16-18-14-8-5-11(2)9-13(14)15(19)20-16/h3-9H,1-2H3,(H,17,18)
InChI key:InChIKey=GFWNGVKCDGYFKG-UHFFFAOYSA-N
SMILES:O=C1C=2C(N=C(NC3=CC=C(C)C=C3)O1)=CC=C(C)C2
Synonyms:- 4H-3,1-Benzoxazin-4-one, 6-methyl-2-[(4-methylphenyl)amino]-
- 6-methyl-2-(4-toluidino)-4H-3,1-benzoxazin-4-one
- Urb 754
- Urb754
- 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
- -tolylamino)-4
- 6-Methyl-2-(p-tolylaMino)-4H-benzo[d][1,3]oxazin-4-one
- 6-Methyl-2-[(4-methylphenyl)amino]-4H-3,1-benzoxazine-4-one
- -3,1-benzoxazin-4-one
- H
- p
- URB754, >=98%
- 6-Methyl-2-(p-tolylamino)-4H-3,1-benzoxazin-4-one
- 6-Methyl-2-(
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Found 5 products.
6-Methyl-2-(p-tolylamino)-4H-3,1-benzoxazin-4-one
CAS:Formula:C16H14N2O2Purity:>95.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:266.30URB754
CAS:<p>"URB754 inhibits rat MAGL with an IC50 of 200 nM, possibly due to impurity. Weak FAAH and CB1 binding, no COX inhibition. Potential pain management target."</p>Formula:C16H14N2O2Color and Shape:SolidMolecular weight:266.29URB754
CAS:Controlled Product<p>Applications 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.<br>References Makara, J.K., et al.: Nat. Neurosci., 8, 1139 (2005)<br></p>Formula:C16H14N2O2Color and Shape:NeatMolecular weight:266.29URB754
CAS:Controlled Product<p>URB754 is a synthetic cannabinoid that inhibits enzyme activity by binding to the serine protease, lipoprotein lipase, and fatty acid amide hydrolase. It also has been shown to have anti-inflammatory effects in cell cultures. URB754 is synthesized from the natural endocannabinoid anandamide by blocking its reuptake and degradation. It can be used to treat metabolic disorders such as diabetes and obesity.</p>Formula:C16H14N2O2Purity:Min. 95%Molecular weight:266.29 g/mol




