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Tilting the Scales toward EGFR Mutant Selectivity: Expanding the Scope of Bivalent "Type V" Kinase Inhibitors

Wittlinger F, Chitnis SP, Pham CD, … Heppner DE · J Med Chem 2024 · J Med Chem 67(23):21438-21469

EGFR and EGFR mutants Tyrosine kinase Inhibitor discovery & SARSelectivity & kinome profilingMechanism & structural biology PhosphoSens

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More publications on EGFR

Enozertinib Is a Selective, Brain-Penetrant EGFR Inhibitor for Treating Non-Small Cell Lung Cancers with EGFR Exon 20 and Atypical Mutations

Junttila MR, Repellin CE, Salaniwal S, … Friedman LS · Cancer Res 2026

Structural Studies of Fourth-Generation EGFR Inhibitors Reveal Insights into Selective T790M and C797S Targeting

Damghani T, Song S, Lin KS, … Heppner DE · ACS Med Chem Lett 2026

TAS3351 is a brain penetrable EGFR-TKI that overcomes T790M and C797S resistant mutations

Kasuga H, Kataoka Y, Yamamoto F, … Mizuarai S · Commun Med (Lond) 2026

Covalent Alkynylpyridopyrimidinones Targeting Cysteine 775 of the Epidermal Growth Factor Receptor Overcome Resistance to Current Therapies

Stewart HL, Bordoni C, Jennings CE, … Waring MJ · J Med Chem 2025

Discovery of STX-721, a Covalent, Potent, and Highly Mutant-Selective EGFR/HER2 Exon20 Insertion Inhibitor for the Treatment of Non-Small Cell Lung Cancer

Milgram BC, Borrelli DR, Brooijmans N, … Guzman-Perez A · J Med Chem 2025

Factors affecting irreversible inhibition of EGFR and influence of chirality on covalent binding

Morese PA, Ahmad A, Martin MP, … Waring MJ · Commun Chem 2025

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