Crizotinib (PF-02341066) is an orally bioavailable, ATP-competitive ALK and c-Met inhibitor with IC50s of 20 and 8 nM, respectively. Crizotinib inhibits tyrosine phosphorylation of NPM-ALK and tyrosine phosphorylation of c-Met with IC50s of 24 and 11 nM in cell-based assays, respectively. Crizotinib is also a ROS1 inhibitor. Crizotinib has effective tumor growth inhibition[1][2][3].
Molekulargewicht:
450.34
Reinheit:
99.97
CAS Nummer:
[877399-52-5]
Formel:
C21H22Cl2FN5O
Target-Kategorie:
Anaplastic lymphoma kinase (ALK),c-Met/HGFR,Ligands for Target Protein for PROTAC,ROS Kinase
Anwendungsbeschreibung:
MCE Product type: Reference compound1
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