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PotentKCa3.1channelblocker(IC50valuesare9,14and15nMforrat,humanandmouseerythrocyteKCa3.1channelsrespectively).Exhibits~50%inhibitionofKCa1.1,KV1.3,andKV11.1channels,noradrenalineanddopaminetransporters,L-typeCa2+channelsandmelatoninreceptorsataconcentrationof10μM.PotentlyinhibitsIL-2andIFN-γproductioninratlymphocytes(IC50~50nM);reducesDBNS-inducedexperimentalcolitisinrats.
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight323.33.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Strøbæketal(2013)NS6180,anewKCa3.1channelinhibitorpreventsT-cellactivationandinflammationinaratmodelofinflammatoryboweldisease.Br.J.Pharmacol.168432PMID:22891655
Keywords:NS6180,supplier,NS6180,KCa3.1,potassium,channels,blockers,inhibitors,inhibits,potent,inflammatory,bowel,disease,gardos,channel,KCNN4,anti-inflammatory,Ca2+-Activated,Potassium,Channels,Ca2+-Activated,Potassium,Channels,TocrisBioscience
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