
CAS 2244904-70-7
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6 produits concernés.
(R)-6,7-Dimethoxy-2-Methyl-N-(1-(4-(2-((Methylamino)Methyl)Phenyl)Thiophen-2-Yl)Ethyl)Quinazolin-4-Amine
CAS :(R)-6,7-Dimethoxy-2-Methyl-N-(1-(4-(2-((Methylamino)Methyl)Phenyl)Thiophen-2-Yl)Ethyl)Quinazolin-4-AmineDegré de pureté :98%Masse moléculaire :448.58g/molBAY-293
CAS :<p>BAY-293 is a potent, cell-active SOS1 inhibitor that disrupts the KRAS-SOS1 interaction (IC50: 21 nM).</p>Formule :C25H28N4O2SDegré de pureté :97.16%Couleur et forme :SolidMasse moléculaire :448.58(R)-6,7-Dimethoxy-2-methyl-N-(1-(4-(2-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)quinazolin-4-amine
CAS :Degré de pureté :98.0%Couleur et forme :Liquid, No data available.Masse moléculaire :448.58999633789066,7-Dimethoxy-2-methyl-N-[(1R)-1-[4-[2-[(methylamino)methyl]phenyl]-2-thienyl]ethyl]-4-quinazolinamine
CAS :Produit contrôléFormule :C25H28N4O2SCouleur et forme :NeatMasse moléculaire :448.58BAY 293
CAS :<p>BAY 293 is a tyrosine kinase inhibitor that blocks the epidermal growth factor receptor (EGFR) and prevents it from binding to the epidermal growth factor (EGF). The BAY 293 also inhibits the activity of other protein kinases, such as Shp2, which are involved in signal transduction pathways. It has been shown to inhibit tumor formation in mice with sarcoma viral oncogene-induced tumors. BAY 293 binds covalently to the enzyme, thereby inhibiting its function. This compound has been shown to be effective against cancer cells that have overactive EGFR and Shp2 proteins.</p>Formule :C25H28N4O2SDegré de pureté :Min. 95%Masse moléculaire :448.59 g/mol




