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Ketaminemetabolite.EnhancesAMPAreceptor-mediatedexcitatorypost-synapticpotentialsintheCA1regionofhippocampalslices.DecreasesintracellularD-serine(aNMDAco-agonist)concentrationsinPC-12cells(IC50=0.68nM).Exertsantidepressanteffectsinmice.Lacksketamine-relatedsideeffects.
SoldunderlicensefromtheNIH,USpatent62/313,309
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight276.16.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Singhetal(2016)KetaminemetabolitesenantioselectivelydecreaseintracellularD-serineconcentrationsinPC-12cells.PLoSOne11e0149499PMID:27096720
Zanosetal(2016)NMDARinhibition-independentantidepressantactionsofketaminemetabolites.Nature533481PMID:27144355
Keywords:2R,6R-Hydroxynorketaminehydrochloride,supplier,Potent,AMPA,agonists,agonism,ketamine,metabolites,antidepressants,ketamine,enantiomer,APJ,2R,6R-HNK,AMPA,Receptors,Ketamine,and,Metabolites,Ketamine,and,Metabolites,TocrisBioscience
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