Synthesis of amide derivatives containing the imidazole moiety and evaluation of their anti‐cardiac fibrosis activity

Abstract

AbstractThree series of N‐{[4‐([1,2,4]triazolo[1,5‐α]pyridin‐6‐yl)‐5‐(6‐methylpyridin‐2‐yl)‐1H‐imidazol‐2‐yl]methyl}acetamides (14a–d, 15a–n, and 16a–f) were synthesized and evaluated for activin receptor‐like kinase 5 (ALK5) inhibitory activities in an enzymatic assay. The target compounds showed high ALK5 inhibitory activity and selectivity. The half maximal inhibitory concentration (IC50) for phosphorylation of ALK5 of 16f (9.1 nM), the most potent compound, was 2.7 times that of the clinical candidate EW‐7197 (vactosertib) and 14 times that of the clinical candidate LY‐2157299. The selectivity index of 16f against p38α mitogen‐activated protein kinase was >109, which was much higher than that of positive controls (EW‐7197: >41, and LY‐2157299: 4). Furthermore, a molecular docking study provided the interaction modes between the target compounds and ALK5. Compounds 14c, 14d, and 16f effectively inhibited the protein expression of α‐smooth muscle actin (α‐SMA), collagen I, and tissue inhibitor of metalloproteinase 1 (TIMP‐1)/matrix metalloproteinase 13 (MMP‐13) in transforming growth factor‐β‐induced human umbilical vein endothelial cells. Compounds 14c and 16f showed especially high activity at low concentrations, which suggests that these compounds could inhibit myocardial cell fibrosis. Compounds 14c, 14d, and 16f are potential preclinical candidates for the treatment of cardiac fibrosis.