Current Trends In Development Of Egfr Inhibitors As A Promising Anticancer Agents: Sar And Synthetic Studies From (2010-2020)

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 seen as a sensible and beneficial strategy in cancer therapy. This review highlighted the most potent EGFR inhibitors with SAR studies and their chemical synthetic pathways discovered between 2010-2020, employed for the treatment of Liver, Breast, Lung, Pancreatic, and Colorectal cancers. We also include the clinical trials as well as the registered patents in our review.