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Antidiabeticagent;bindstoPPARγandpotentlyinhibitsCdk5-mediatedPPARγphosphorylation(IC50=80nM;Ki=28.67nM)withoutexhibitingPPARγagoNISTactivity.DoesnotinhibitCdk5-dependentphosphorylationofRb.Reducesfastinginsulinlevelsandimprovesinsulinsensitivityinamousemodelofdiabetes.
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight547.6.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
NorrisandSigmund(2012)AsecondchanceforaPPARγtargetedtherapy?Circ.Res.1108PMID:22223206
Choietal(2011)Antidiabeticactionsofanon-agonistPPARγligandblockingCdk5-mediatedphosphorylation.Nature477477PMID:21892191
Keywords:SR1664,supplier,SR1664,antidiabetics,diabetes,PPARgamma,PPARg,peroxisome,proliferator,activated,receptor,ligand,Cdk5,phosphorylation,LBD,PPARgamma,Receptors,PPARgamma,Receptors,TocrisBioscience
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