Synthesis and c-Src inhibitory activity of imidazo[1,5-a]pyrazine derivatives as an agent for treatment of acute ischemic stroke

We synthesized and evaluated a series of C-5 substituted imidazo[1,5-a]pyrazine derivatives to identify potent c-Src inhibitors as potential therapeutic agents for acute ischemic stroke. Among these compounds, compound 14c·HCl demonstrated remarkable central nervous system (CNS) penetration and significant neuroprotective efficacy in vivo in rat models.

We studied novel c-Src inhibitors as potential therapeutic agents for acute ischemic stroke. Compound 14c·HCl demonstrated potent c-Src inhibitory activity, remarkable central nervous system (CNS) penetration, and significant neuroprotective efficacy in vivo in rat models.Figure optionsDownload as PowerPoint slide