New imidazo[1,2-a]quinoxaline derivatives: Synthesis and in vitro activity against human melanoma

New imidazo[1,2-a]quinoxaline analogues have been synthesized in good yields via a bimolecular condensation of 2-imidazole carboxylic acid, followed by a coupling with ortho-fluoroaniline and subsequent substitution on the imidazole ring by Suzuki Cross-coupling reaction using microwave assistance. Antitumor activities of these derivatives were evaluated by growth inhibition of A375 cells in vitro. All compounds exhibited high activities compared to imiquimod and fotemustine used as references.

IC50 against A375: 0.20 ± 0.09 μM.Figure optionsDownload as PowerPoint slide