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Orallyactiveinhibitoroflipocalin-typeprostaglandinDsynthase(L-PGDS)(Ki=75μM,IC50=95μM).InhibitstheproductionofPGD2fromPGH2invitro,withnoeffectonPGE2orPGF2αproduction.
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight397.52.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Irikuraetal(2009)Biochemical,functionalandpharmacologicalcharacterizationofAT-56,anorallyactiveandselectiveinhibitoroflipocalin-typeprostaglandinDsynthase.J.Biol.Chem.2847623PMID:19131342
Keywords:AT56,supplier,AT56,L-PGDS,lipocalin-type,prostaglandin,PG,D,synthase,inhibitors,inhibits,Other,Synthases/Synthetases,Other,Synthases/Synthetases,TocrisBioscience
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