Antitumor Activity of HKI-272, an Orally Active, Irreversible Inhibitor of the HER-2 Tyrosine Kinase
By S. Rabindran, C. Discafani, E. Rosfjord, M. Baxter, M. Floyd, J. Golas, W. Hallett, Bernard D. Johnson, R. Nilakantan, E. Overbeek and 6 more. Cancer Research, 2004
625 citations recorded by the source corpus.
Subfields: Oncology, Radiology, Nuclear Medicine and Imaging
View Paper: https://www.semanticscholar.org/paper/abf1a9d54a2c3abc10214bebcd85182b601f9be3
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In Oncology
In Radiology, Nuclear Medicine and Imaging
Citations in the corpus
- Kinase-targeted cancer therapies: progress, challenges and future directions (2018, background): “The covalent kinase inhibitors bind to a cysteine residue in or around the active site, thus preventing the binding of ATP to the protein kinase [117, 127].”
- BIBW2992, an irreversible EGFR/HER2 inhibitor highly effective in preclinical lung cancer models (2008, background): “ATP-binding site of the kinase domains of EGFR (Cys 773) and HER2 (Cys 805) (Rabindran et al., 2004; Eskens et al., 2008).”
- Targeting the PI5P4K lipid kinase family in cancer using covalent inhibitors (2020, background): “, 2007), EGFR inhibitors neratinib (Rabindran et al., 2004), afatinib (Li et al.”
- Epidermal growth factor receptor mutations in lung cancer (2007, background): “Previous studies from our laboratory have shown that the irreversible dual EGFR and ERBB2 inhibitors, HKI-272 (Ref”