Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.
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Erlotinib is an EGFR inhibitor (Ki = 2.7 nM).1 It is greater than 1,000-fold selective for EGFR over Src and Abl at 0.1 µM.2 Erlotinib induces caspase-3 and -7 activity in NCI H358 non-small cell lung cancer (NSCLC) cells when used at a concentration of 1 µM.3 Erlotinib (25 mg/kg) reduces EGF-induced EGFR autophosphorylation in an HN-5 head and neck cancer mouse xenograft model.2 Formulations containing erlotinib have been used in the treatment of various cancers.
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1. A novel approach in the treatment of cancer: Targeting the epidermal growth factor receptor. Clin. Cancer Res. 7(10), 2958-2970 (2001).
2. Induction of apoptosis and cell cycle arrest by CP-
3. Targeting the epidermal growth factor receptor in non-