Synthesis and biological evaluation of benzamides and benzamidines: structural requirement of a pyrimidine ring for inhibition of EGFR tyrosine kinase

Abstract

The benzamides 1 and the benzamidines 2–3 were synthesized as the mimics of 4-anilinoquinazolines, which possess inhibition of epidermal growth factor receptor (EGFR) tyrosine kinase, and tested for cytotoxicity toward A431 and inhibitory activity toward autophosphorylation by the enzyme assay. High cell growth inhibition was observed in a series of the cyclic benzamides 3: the IC50 values are 0.09–0.32mM. The benzamidines 3a and 3b exhibited high inhibition of EGFR tyrosine kinase at a 1.0μM concentration, although the benzamides 1 and the benzamidines 2 did not show significant kinase inhibition at a 10μM concentration.