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URB-602

Structure via PubChem · Public domain (PubChem)

EntityQ7865593· pop 6· linked from 502 articles

Also known as URB602, URB 602

URB602 ([1,1'-biphenyl]-3-yl-carbamic acid, cyclohexyl ester) is a compound that has been found to inhibit hydrolysis of monoacyl glycerol compounds, such as 2-arachidonoylglycerol (2-AG) and 2-oleoylglycerol (2-OG). It was first described in 2003. A study performed in 2005 found that the compound had specificity for metabolizing 2-AG over anandamide (another cannabinoid ligand) in rat brain presumably by inhibiting the enzyme monoacylglycerol lipase (MAGL), which is the primary metabolic enzyme of 2-AG. However, subsequent studies have shown that URB602 lacks specificity for MAGL inhibition i

Chemical data

Formula
C19H21NO2
Molecular weight
295.4 g/mol
IUPAC name
cyclohexyl N-(3-phenylphenyl)carbamate

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

~1 min read

Encyclopedic overview

1 sections
Contents
  • References

URB602 ([1,1'-biphenyl]-3-yl-carbamic acid, cyclohexyl ester) is a compound that has been found to inhibit hydrolysis of monoacyl glycerol compounds, such as 2-arachidonoylglycerol (2-AG) and 2-oleoylglycerol (2-OG). It was first described in 2003. A study performed in 2005 found that the compound had specificity for metabolizing 2-AG over anandamide (another cannabinoid ligand) in rat brain presumably by inhibiting the enzyme monoacylglycerol lipase (MAGL), which is the primary metabolic enzyme of 2-AG. However, subsequent studies have shown that URB602 lacks specificity for MAGL inhibition in vitro.

==References==

Excerpted from Wikipedia’s “URB-602” article, available under the CC BY-SA 4.0 licence.

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