article · Journal of Enzyme Inhibition and Medicinal Chemistry
The abstract on record is too brief for a reliable plain-language summary, so none has been generated.
were assessed for their EGFR kinase (Wild and T790M) inhibitory activities, revealing eligible potential. Additionally, molecular docking, ADME, and SAR studies were carried out for the investigated candidates.
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DOI: 10.1080/14756366.2022.2135512
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