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Ahighaffinityblockerforinward-rectifierK+channels,thiscompoundisastablederivativeofthebeevenomtoxintertiapin.BindstoROMK1(Kir1.1)andGIRK1/4(Kir3.1/3.4)channelswithhighaffinity(Kivaluesare1.3and13.3nMrespectively)andisselectiveoverKir2.1channels.DerivativetertiapinLQ(Cat.No.4339)alsoavailable.
SoldunderlicensegrantedbytheUniversityofPennsylvania
(Modifications:Disulfidebridgebetween3-14,5-18,Lys-21=C-terminalamide)
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight2452.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Jinetal(1999)Mechanismsofinward-rectifierK+channelinhibitionbytertiapin-Q.Biochemistry3814294PMID:10572004
JinandLu(1999)Synthesisofastableformoftertiapin:ahigh-affinityinhibitorforinward-rectifierK+channels.Biochemistry3814286PMID:10572003
Keywords:Tertiapin-Q,supplier,Potent,selective,blockers,inward-rectifier,K+,channels,Potassium,KIR,Channels,venoms,Inward,rectifier,Potassium,Channels,Inward,rectifier,Potassium,Channels,TocrisBioscience
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