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N-oxide alkaloids from Crinum amabile (Amaryllidaceae)

Natural products play an important role in the development of new drugs. In this context, the Amaryllidaceae alkaloids have attracted considerable attention in view of their unique structural features and various biological activities. In this study, twenty-three alkaloids were identified from Crinu...

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Detalles Bibliográficos
Autores principales: Tallini, Luciana R., Torras-Claveria, Laura, Borges, Warley de Souza, Kaiser, Marcel, Viladomat, Francesc, Zuanazzi, José Angelo S., Bastida, Jaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099558/
https://www.ncbi.nlm.nih.gov/pubmed/29861456
http://dx.doi.org/10.3390/molecules23061277
Descripción
Sumario:Natural products play an important role in the development of new drugs. In this context, the Amaryllidaceae alkaloids have attracted considerable attention in view of their unique structural features and various biological activities. In this study, twenty-three alkaloids were identified from Crinum amabile by GC-MS and two new structures (augustine N-oxide and buphanisine N-oxide) were structurally elucidated by NMR. Anti-parasitic and cholinesterase (AChE and BuChE) inhibitory activities of six alkaloids isolated from this species, including the two new compounds, are described herein. None of the alkaloids isolated from C. amabile gave better results than the reference drugs, so it was possible to conclude that the N-oxide group does not increase their therapeutic potential.