Product Data Sheet

Crizotinib-d9

Catalog No. B15038

main product photo
Crizotinib-d9 (PF-02341066-d9) is a deuterium-labeled derivative of Crizotinib, designed for use as a stable isotope in chemical research. Crizotinib is an orally bioavailable, ATP-competitive inhibitor targeting ALK and c-Met, exhibiting IC50 values of 20 nM and 8 nM, respectively. It is known to effectively inhibit tyrosine phosphorylation of NPM-ALK and c-Met in cell-based assays, with IC50 values of 24 nM and 11 nM. Additionally, Crizotinib serves as a ROS1 inhibitor and demonstrates significant tumor growth inhibition, making it crucial for oncology research applications.
Chemical Information
Catalog NumB15038
M. Wt459.39
FormulaC21H13D9Cl2FN5O
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.1523580-59-7
SynonymsPF-02341066-d9
SMILESC[C@H](C1=C(C(F)=CC=C1Cl)Cl)OC2=CC(C3=CN(C4([2H])C([2H])([2H])C([2H])([2H])NC([2H])([2H])C4([2H])[2H])N=C3)=CN=C2N
Biological Activity
DescriptionCrizotinib-d9 (PF-02341066-d9) is a deuterium-labeled derivative of Crizotinib, designed for use as a stable isotope in chemical research. Crizotinib is an orally bioavailable, ATP-competitive inhibitor targeting ALK and c-Met, exhibiting IC50 values of 20 nM and 8 nM, respectively. It is known to effectively inhibit tyrosine phosphorylation of NPM-ALK and c-Met in cell-based assays, with IC50 values of 24 nM and 11 nM. Additionally, Crizotinib serves as a ROS1 inhibitor and demonstrates significant tumor growth inhibition, making it crucial for oncology research applications.
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SHIPPING AND STORAGE
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