Xanthone and Flavone Derivatives as Dual Agents with Acetylcholinesterase Inhibition and Antioxidant Activity as Potential Anti-Alzheimer Agents

• Tipo: Artigo em Revista Científica Internacional
• Data: 2017

Autores

Cruz, I (Autor) Outra; Puthongking, P (Autor) Outra; Sara Cravo (Autor) FFUP; Palmeira, A (Autor) FFUP; Honorina Cidade (Autor) FFUP; Pinto, M (Autor) Outra; Emilia Sousa (Autor) FFUP

Revista

Título: Journal of Chemistry

Vol. 2017

Páginas: 1-16

ISSN: 2090-9063

Editora: Hindawi

Indexação

ISI Web of Knowledge - 30 Citações

Scopus - 0 Citações

Outras Informações

ID Authenticus: P-00M-QCY

DOI: 10.1155/2017/8587260

Abstract (EN): Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder that is associated with the elderly. The current therapy that is used to treat AD is based mainly on the administration of acetylcholinesterase (AChE) inhibitors. Due to their low efficacy there is a considerable need for other therapeutic strategies. Considering that the malfunctions of different, but interconnected, biochemical complex pathways play an important role in the pathogenesis of this disease, a promising therapy may consist in administration of drugs that act on more than a target on biochemical scenery of AD. In this work, the synthesis and evaluation of xanthone and flavone derivatives as antioxidants with AChE inhibitory activity were accomplished. Among the obtained compounds, Mannich bases 3 and 14 showed capacity to inhibit AChE and antioxidant property, exerting dual activity. Moreover, for the most promising AChE inhibitors, docking studies on the target have been performed aiming to predict the binding mechanism. The results presented here may help to identify new xanthone and flavone derivatives as dual anti-Alzheimer agents with AChE inhibitory and antioxidant activities.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 16