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Xanthenedione derivatives, new promising antioxidant and acetylcholinesterase inhibitor agents

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Molecules 2014 19 8317-8333 publicado.pdf343.2 KBAdobe PDF Download

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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).

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Xanthene-1,9(2H)-diones Scavenging Activity Reduction Power Acetylcholinesterase Inhibitors Xanthones 3-cinnamoyl-5-hydroxy-2-styrylchromones

Citation

Seca, Ana; Leal, Stephanie; Pinto, Diana; Barreto, Maria; Silva, Artur (2014). "Xanthenedione derivatives, new promising antioxidant and acetylcholinesterase inhibitor agents", Molecules, 19(6), 8317-8333. Doi: 10.3390/molecules19068317.

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