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LSD1inhibitor(IC50=990nM;Ki=610nM).ExhibitsselectivityforLSD1overMAO-BandMAO-A(Kivaluesare17and110μM,respectively).
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight311.75.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Mimasuetal(2010)Structurallydesignedtrans-2-phenylcyclopropylaminederivativespotentlyinhibithistonedemethylaseLSD1/KDM1.Biochemistry496494PMID:20568732
Keywords:S2101,supplier,S2101,LSD1,inhibitors,inhibits,histones,demethylases,KDM1,Histone,Demethylases,Histone,Demethylases,TocrisBioscience
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