Molecules (May 2018)

N-oxide alkaloids from Crinum amabile (Amaryllidaceae)

  • Luciana R. Tallini,
  • Laura Torras-Claveria,
  • Warley de Souza Borges,
  • Marcel Kaiser,
  • Francesc Viladomat,
  • José Angelo S. Zuanazzi,
  • Jaume Bastida

DOI
https://doi.org/10.3390/molecules23061277
Journal volume & issue
Vol. 23, no. 6
p. 1277

Abstract

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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.

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