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URB602

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URB602
Names

Preferred IUPAC name Cyclohexyl ([1,1′-biphenyl]-3-yl)carbamate
Other names [1,1′-Biphenyl]-3-yl-carbamic acid, cyclohexyl ester
Identifiers
CAS Number	565460-15-3^Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL77767^Y
ChemSpider	9154538^Y
PubChem CID	10979337
UNII	B8371SFA9K^Y
CompTox Dashboard(EPA)	DTXSID90450611
InChI InChI=1S/C19H21NO2/c21-19(22-18-12-5-2-6-13-18)20-17-11-7-10-16(14-17)15-8-3-1-4-9-15/h1,3-4,7-11,14,18H,2,5-6,12-13H2,(H,20,21)^Y Key: HHVUFQYJOSFTEH-UHFFFAOYSA-N^Y
SMILES O=C(OC1CCCCC1)Nc1cccc(c1)c1ccccc1
Properties
Chemical formula	C₁₉H₂₁NO₂
Molar mass	295.382 g·mol⁻¹
Appearance	Crystalline solid
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references

Chemical compound

URB602 ([1,1'-biphenyl]-3-yl-carbamic acid, cyclohexyl ester) is a compound that has been found to inhibithydrolysis ofmonoacyl glycerol compounds, such as2-arachidonoylglycerol (2-AG) and2-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 overanandamide (anothercannabinoid ligand) in rat brain presumably by inhibiting the enzymemonoacylglycerol lipase (MAGL), which is the primary metabolic enzyme of 2-AG.^[2] However, subsequent studies have shown that URB602 lacks specificity for MAGL inhibitionin vitro.^[3]

References

[edit]

^Tarzia, G; Duranti, A; Tontini, A; Piersanti, G; Mor, M; Rivara, S; Plazzi, PV; Park, C; et al. (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.S2CID 30528443.
^Hohmann, Andrea G.; Suplita, Richard L.; Bolton, Nathan M.; Neely, Mark H.; Fegley, Darren; Mangieri, Regina; Krey, Jocelyn F.; Michael Walker, J.; et al. (2005)."An endocannabinoid mechanism for stress-induced analgesia"(PDF).Nature.435 (7045):1108–12.Bibcode:2005Natur.435.1108H.doi:10.1038/nature03658.PMID 15973410.S2CID 4339948.
^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.

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