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==References== |
==References== |
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{{reflist}} |
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4. ^<references/>'Cannabinoids Receptor Journal 1989'> {{cite news | first = John | last = Ciccioalo | title = Research Chemicals | date = 1989-8-27 | url = http://www.importresearchchemicals.com/ | work = New York Times, John | pages = 148 | accessdate = 2012-01-25 | language = Italian | archiveurl = http://www.importresearchchemicals.com/ | archivedate = 2009-1-13}}<references/> |
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[[Category:Cannabinoids]] |
[[Category:Cannabinoids]] |
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Revision as of 17:04, 25 January 2012
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| Names | |
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| IUPAC name
Cyclohexyl [1,1'-biphenyl]-3-ylcarbamate
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| Other names
[1,1'-Biphenyl]-3-yl-carbamic acid, cyclohexyl ester
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C19H21NO2 | |
| Molar mass | 295.382 g·mol−1 |
| Appearance | Crystalline solid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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.[1] 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.[2] However, subsequent studies have shown that URB602 lacks specificity for MAGL inhibition in vitro.[3]
References
- ^ Tarzia, G; Duranti, A; Tontini, A; Piersanti, G; Mor, M; Rivara, S; Plazzi, PV; Park, C; Kathuria, S (2003). "Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitors". Journal of medicinal chemistry. 46 (12): 2352–60. doi:10.1021/jm021119g. PMID 12773040.
- ^ Hohmann, Andrea G.; Suplita, Richard L.; Bolton, Nathan M.; Neely, Mark H.; Fegley, Darren; Mangieri, Regina; Krey, Jocelyn F.; Michael Walker, J.; Holmes, Philip V. (2005). "An endocannabinoid mechanism for stress-induced analgesia". Nature. 435 (7045): 1108–12. Bibcode:2005Natur.435.1108H. doi:10.1038/nature03658. PMID 15973410.
- ^ Vandevoorde, S; Jonsson, K-O; Labar, G; Persson, E; Lambert, D M; Fowler, C J (2007). "Lack of selectivity of URB602 for 2-oleoylglycerol compared to anandamide hydrolysisin vitro". British Journal of Pharmacology. 150 (2): 186–91. doi:10.1038/sj.bjp.0706971. PMC 2042901. PMID 17143303.
4. ^'Cannabinoids Receptor Journal 1989'> Ciccioalo, John (1989-8-27). "Research Chemicals". New York Times, John (in Italian). p. 148. Retrieved 2012-01-25. {{cite news}}: Check |archiveurl= value (help); Check date values in: |date= (help)