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PotentandselectivePPARδagonist(EC50=1.2nM).Displays<1000-fold selectivity="" over="" other="" ppar="" subtypes.="" increases="" abc="" a1="" transporter="" expression="" and="" induces="" apolipoprotein="" a1-mediated="" cholesterol="" efflux="">1000-fold>invitro.AlsoincreaseserumHDLcholesterolandlowerssmall,denseLDLlevelsinobesityinvivomodels.
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight453.5.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Oliveretal(2001)Aselectiveperoxisomeproliferator-activatedreceptordeltaagonistpromotesreversecholesteroltransport.Proc.Natl.Acad.Sci.USA.985306PMID:11309497
Itoetal(2016)Self-renewalofapurifiedTie2+hematopoieticstemcellpopulationreliesonmitochondrialclearance.Science3541156PMID:27738012
Keywords:GW501516,supplier,GW501516,Potent,selective,PPARδ,agonists,agonism,reverse,cholesterol,transporter,ATP-binding,cassette,A1,obesity,peroxisome,proliferator-activated,receptors,delta,PPARdelta,Receptors,PPARdelta,Receptors,TocrisBioscience
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