Theoretical and Natural Science
- The Open Access Proceedings Series for Conferences
Vol. 35, 10 July 2024
* Author to whom correspondence should be addressed.
Inhibitors of the epidermal growth factor receptor (EGFR) have been approved as drugs to treat patients with non-small-cell lung cancer (NSCLC). While these medications exhibit good clinical efficacy, a lot of patients acquire treatment resistance due to T790M mutation, causing the disease to advance. Furthermore, these medicines may hit the EGFR wild-type receptor, leading to adverse effects. In this publication, we present the discovery of the medication osimertinib (AZD9291), a mutant-selective agent. The T790M resistant mutant and EGFR sensitizing (or activating, EGFRm+) mutant are both irreversibly inhibited. In addition, it possesses high selectivity to the receptor's wild-type form.
osimertinib (AZD9291), epidermal growth factor receptor (EGFR), tyrosine kinase inhibitors, drug resistance, anticancer
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The datasets used and/or analyzed during the current study will be available from the authors upon reasonable request.
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