Product Data Sheet

Erlotinib-d4

Catalog No. A28598

main product photo
Erlotinib-d4 is a deuterium-labeled analog of Erlotinib, a selective inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase, with an IC50 of 2 nM for human EGFR. This compound effectively reduces EGFR autophosphorylation in intact tumor cells with an IC50 of 20 nM and is utilized in the treatment of non-small cell lung cancer. Additionally, Erlotinib-d4 serves as a valuable click chemistry reagent, featuring an alkyne group for performing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules, facilitating various biochemical applications.
Chemical Information
Catalog NumA28598
M. Wt397.46
FormulaC22H19D4N3O4
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.1130852-41-3
SynonymsCP-358774-d4; NSC 718781-d4; OSI-774-d4
SMILESCOCCOC(C(OCCOC)=C1)=CC2=C1C(NC3=C([2H])C(C#C)=C([2H])C([2H])=C3[2H])=NC=N2
Biological Activity
DescriptionErlotinib-d4 is a deuterium-labeled analog of Erlotinib, a selective inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase, with an IC50 of 2 nM for human EGFR. This compound effectively reduces EGFR autophosphorylation in intact tumor cells with an IC50 of 20 nM and is utilized in the treatment of non-small cell lung cancer. Additionally, Erlotinib-d4 serves as a valuable click chemistry reagent, featuring an alkyne group for performing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules, facilitating various biochemical applications.
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SHIPPING AND STORAGE
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