Résumé
A series of 1,4-disubstituted 1,2,3-triazoles derivatives (3) were designed and prepared as potential inhibitors for Src kinase. In this manuscript, all of the designed compounds were screened via molecular docking using PLANTS as virtual screening software to identify new inhibitors of Src kinase. As expected, the results of the docking study revealed that most of these targeted compounds possessed low binding energy. Subsequently, all of the screened compounds were synthesized via Huisgen's 1,3-dipolar cycloaddition between terminal alkynes (1) and methyl 2-azidoacetate (2) with Cu(I) in excellent yields at room temperature. The synthesized triazoles (3) were characterized by IR, 1 H, 13 C, 19 F NMR and mass spectral techniques and they were investigated as inhibitors of Src kinase. Among these compounds, 3m exhibited the most potent inhibitory activity against Src kinase.