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Metabolicallystableinhibitorofanandamidecellularuptake(Ki=3μM).DisplaysrelativelylowaffinityforCB1andCB2receptors(Kivaluesare5.1and>10μM)andforvanilloidVR1receptors(EC50=10μM).HasminimalactivityagainstFAAH(Ki>50μM).Activeinvivo.
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight431.66.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Ortaretal(2003)Novelselectiveandmetabolicallystableinhibitorsofanandamidecellularuptake.Biochem.Pharmacol.351473PMID:12732359
deLagoetal(2004)Invivopharmacologicalactionsoftwonovelinhibitorsofanandamidecellularuptake.Eur.J.Pharmacol.484249PMID:14744610
Keywords:OMDM-2,supplier,Potent,inhibitors,inhibits,anandamide,reuptake,AMT,Transporters,cannABInoids,Monoamine,Neurotransmitter,Cannabinoid,Transporters,Cannabinoid,Transporters,TocrisBioscience
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