Xanthenedione derivatives, new promising antioxidant and acetylcholinesterase inhibitor agents

• Autor(a) principal: Seca, Ana M. L.
• Data de Publicação: 2014
• Outros Autores: Leal, Stephanie B., Pinto, Diana C. G. A., Barreto, Maria do Carmo, Silva, Artur M. S.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10400.3/3182
• topic: Xanthene-1,9(2H)-diones; Xanthones; 3-cinnamoyl-5-hydroxy-2-styrylchromones; Scavenging Activity; Reduction Power; Acetylcholinesterase Inhibitors

Natural and synthetic xanthone derivatives are well-known for their ability to act as antioxidants and/or enzyme inhibitors. This paper aims to present a successful synthetic methodology towards xanthenedione derivatives and the study of their aromatization to xanthones. Additionally their ability to reduce Fe(III), to scavenge DPPH radicals and to inhibit AChE was evaluated. The results demonstrated that xanthenedione derivative 5e, bearing a catechol unit, showed higher reduction capacity than BHT and similar to quercetin, strong DPPH scavenging activity (EC50 = 3.79 ± 0.06 μM) and it was also showed to be a potent AChEI (IC50 = 31.0 ± 0.09 μM) when compared to galantamine (IC50 = 211.8 ± 9.5 μM).