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PotentandselectiveFLT3inhibitor(IC50=40nM).Exhibits>10-foldand170-foldselectivityforFLT3overBTKkinaseandc-KITkinase,respectivelyinvitro.InducesapoptosisbyarrestingcellcycleinG0/G1phaseinvitro.SuppressestumorgrowthinanAMLxenograftmodel.Modestlyorallybioavailable.
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight471.55.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Lietal(2015)Discoveryof(R)-1-(3-(4-Amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)-2-(dimethylamino)ethanone(CHMFL-FLT3-122)asapotentandorallyavailableFLT3kinaseinhibitorforFLT3-ITDpositiveacutemyeloidleuJ.Med.Chem.589625PMID:26630553
Keywords:CHMFL-FLT3-122,supplier,Potent,selective,FLT,inhibitors,inhibits,AML,acute,myeloid,leukemia,cell,cycle,FLT3,Cell,Cycle,Inhibitors,Apoptosis,Inducers,FLT3,TocrisBioscience
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