Abstract
Abstract: The EGFR (Epidermal Growth Factor Receptor) regulates cell proliferation, survival, and differentiation. The EGFR is a cell surface receptor that belongs to the ErbB tyrosine kinase family. One of the most important targets for cancer therapy is EGFR inhibition. Because EGFR over-activation is seen in a wide range of malignancies, targeting EGFR and its downstream signaling cascades is a sensible and beneficial strategy in cancer therapy. This review highlighted the most potent EGFR inhibitors with SAR studies and their synthetic chemical pathways discovered between 2010-2020, employed for treating Liver, Breast, Lung, Pancreatic, and Colorectal cancers. We also include the clinical trials and the registered patents in our review.
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