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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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 |
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author | Tallini, Luciana R. Torras-Claveria, Laura Borges, Warley de Souza Kaiser, Marcel Viladomat, Francesc Zuanazzi, José Angelo S. Bastida, Jaume |
author_facet | Tallini, Luciana R. Torras-Claveria, Laura Borges, Warley de Souza Kaiser, Marcel Viladomat, Francesc Zuanazzi, José Angelo S. Bastida, Jaume |
author_sort | Tallini, Luciana R. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6099558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60995582018-11-13 N-oxide alkaloids from Crinum amabile (Amaryllidaceae) Tallini, Luciana R. Torras-Claveria, Laura Borges, Warley de Souza Kaiser, Marcel Viladomat, Francesc Zuanazzi, José Angelo S. Bastida, Jaume Molecules Article 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. MDPI 2018-05-26 /pmc/articles/PMC6099558/ /pubmed/29861456 http://dx.doi.org/10.3390/molecules23061277 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tallini, Luciana R. Torras-Claveria, Laura Borges, Warley de Souza Kaiser, Marcel Viladomat, Francesc Zuanazzi, José Angelo S. Bastida, Jaume N-oxide alkaloids from Crinum amabile (Amaryllidaceae) |
title | N-oxide alkaloids from Crinum amabile (Amaryllidaceae) |
title_full | N-oxide alkaloids from Crinum amabile (Amaryllidaceae) |
title_fullStr | N-oxide alkaloids from Crinum amabile (Amaryllidaceae) |
title_full_unstemmed | N-oxide alkaloids from Crinum amabile (Amaryllidaceae) |
title_short | N-oxide alkaloids from Crinum amabile (Amaryllidaceae) |
title_sort | n-oxide alkaloids from crinum amabile (amaryllidaceae) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099558/ https://www.ncbi.nlm.nih.gov/pubmed/29861456 http://dx.doi.org/10.3390/molecules23061277 |
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