Synthesis and Evaluation of Novel 1,2,6-Thiadiazinone Kinase Inhibitors as Potent Inhibitors of Solid Tumors
A focused series of substituted 4H-1,2,6-thiadiazin-4-ones was designed and synthesized to probe the anti-cancer GABA properties of this scaffold.Insights from previous kinase inhibitor programs were used to carefully select several different substitution patterns.Compounds were tested on bladder, prostate, pancreatic, breast, chordoma, and lung ca