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Potentandselectivefattyacidamidehydrolase(FAAH)inhibitor(IC50valuesare3and5nMinhumanliverandratbrain,respectively).Exhibitsnosignificantinhibitoryactivityagainstavarietyofreceptors,ionchannelsandenzymes,includinghumancannABInoidreceptorsandratmonoacylglycerollipase.Displaysantiallodynicandantihyperalgesicactivityinaninflammatorypainmodel.
URB597isalsoofferedaspartoftheTocriscreenPlus.FindoutmoreaboutcompoundlibrariesavailablefromTocris.
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight338.4.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Hohmannetal(2005)Anendocannabinoidmechanismforstress-inducedanalgesia.Nature4351108PMID:15973410
Piomellietal(2006)PharmacologicalprofileoftheselectiveFAAHinhibitorKDS-4103(URB597).CNSDrugRev.1221PMID:16834756
Jayamanneetal(2006)ActionsoftheFAAHinhibitorURB597inneuropathicandinflammatorychronicpainmodels.Br.J.Pharmacol.147281PMID:16331291
Keywords:URB597,supplier,URB597,faah,fatty,acid,amide,hydrolase,inhibitors,inhibits,selective,potent,Fatty,Acid,Amide,Hydrolase,(FAAH),Other,Cannabinoids,Fatty,Acid,Amide,Hydrolase,(FAAH),TocrisBioscience
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