Anti-leishmanial and structure-activity relationship of ring substituted 3-phenyl-1 -(1,4-di-N-oxide quinoxalin-2-yl)-2-propen-1-one derivatives

Abstract

A series of ring substituted 3-phenyl-1-(1,4-di-N-oxide quinoxalin-2-yl)-2-propen-1-one derivatives were synthesized and tested for in vitro leishmanicidal activity against amastigotes of Leishmania amazonensis in axenical cultures and murine infected macrophages. Structure-activity relationships demonstrated the importance of a radical methoxy at position R3′, R4′ and R5′. (2E)-3-(3,4,5-trimethoxy-phenyl)-1-(3,6,7-trimethyl-1,4-dioxy-quinoxalin-2-yl) -propenone was the most active. Cytotoxicity on macrophages revealed that this product was almost six times more active than toxic.