Oyebamiji AKAkintelu SAAmao OPKaka MOMorakinyo AEAmao FASemire B2022-07-272022-07-27202110.1016/j.dib.2021.1072342352-3409https://nerd.ethesis.ng/handle/123456789/401Data in BriefData from eight 1,2,4-thiadiazole-1,2,4-triazole derivatives were used to observe the anti-epidermal growth factor receptor kinase activities of 1,2,4-thiadiazole-1,2,4-triazole analogues thereby reducing human lung cancer. The software used to achieve this work were Spartan 14, Pymol, mgltools_win32_1.5.6, Auto dock vina and biovia2019.ds2019client. Also, the developed QSAR model was developed using the screened descriptors so as to inspect the closeness between the experimental IC50 and the predicted IC50. More so, the binding affinity from 1,2,4-thiadiazole-1,2,4-triazole derivatives - epidermal growth factor receptor kinase complexes using molecular docking approach were reported. Also, the ADMET properties for selected compounds and proposed compounds with better binding affinity were reported.en124-ThiadiazoleEGFRK124-TriazoleLung cancerQSARDFTDockingArticle