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Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America

The genus Clinanthus Herb. is found in the Andes Region (South America), mainly in Peru, Ecuador, and Bolivia. These plants belong to the Amaryllidaceae family, specifically the Amaryllidoideae subfamily, which presents an exclusive group of alkaloids known as Amaryllidaceae alkaloids that show impo...

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Autores principales: Rodríguez-Escobar, María Lenny, Tallini, Luciana R., Lisa-Molina, Julia, Berkov, Strahil, Viladomat, Francesc, Meerow, Alan, Bastida, Jaume, Torras-Claveria, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385320/
https://www.ncbi.nlm.nih.gov/pubmed/37513280
http://dx.doi.org/10.3390/molecules28145408
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author Rodríguez-Escobar, María Lenny
Tallini, Luciana R.
Lisa-Molina, Julia
Berkov, Strahil
Viladomat, Francesc
Meerow, Alan
Bastida, Jaume
Torras-Claveria, Laura
author_facet Rodríguez-Escobar, María Lenny
Tallini, Luciana R.
Lisa-Molina, Julia
Berkov, Strahil
Viladomat, Francesc
Meerow, Alan
Bastida, Jaume
Torras-Claveria, Laura
author_sort Rodríguez-Escobar, María Lenny
collection PubMed
description The genus Clinanthus Herb. is found in the Andes Region (South America), mainly in Peru, Ecuador, and Bolivia. These plants belong to the Amaryllidaceae family, specifically the Amaryllidoideae subfamily, which presents an exclusive group of alkaloids known as Amaryllidaceae alkaloids that show important structural diversity and pharmacological properties. It is possible to find some publications in the literature regarding the botanical aspects of Clinanthus species, although there is little information available about their chemical and biological activities. The aim of this work was to obtain the alkaloid profile and the anti-cholinesterase activity of four different samples of Clinanthus collected in South America: Clinanthus sp., Clinanthus incarnatus, and Clinanthus variegatus. The alkaloid extract of each sample was analyzed by gas chromatography coupled with mass spectrometry (GC-MS), and their potential against the enzymes acetyl- and butyrylcholinesterase were evaluated. Thirteen alkaloids have been identified among these species, while six unidentified structures have also been detected in these plants. The alkaloid extract of the C. variegatus samples showed the highest structural diversity as well as the best activity against AChE, which was likely due to the presence of the alkaloid sanguinine. The results suggest this genus as a possible interesting new source of Amaryllidaceae alkaloids, which could contribute to the development of new medicines.
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spelling pubmed-103853202023-07-30 Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America Rodríguez-Escobar, María Lenny Tallini, Luciana R. Lisa-Molina, Julia Berkov, Strahil Viladomat, Francesc Meerow, Alan Bastida, Jaume Torras-Claveria, Laura Molecules Article The genus Clinanthus Herb. is found in the Andes Region (South America), mainly in Peru, Ecuador, and Bolivia. These plants belong to the Amaryllidaceae family, specifically the Amaryllidoideae subfamily, which presents an exclusive group of alkaloids known as Amaryllidaceae alkaloids that show important structural diversity and pharmacological properties. It is possible to find some publications in the literature regarding the botanical aspects of Clinanthus species, although there is little information available about their chemical and biological activities. The aim of this work was to obtain the alkaloid profile and the anti-cholinesterase activity of four different samples of Clinanthus collected in South America: Clinanthus sp., Clinanthus incarnatus, and Clinanthus variegatus. The alkaloid extract of each sample was analyzed by gas chromatography coupled with mass spectrometry (GC-MS), and their potential against the enzymes acetyl- and butyrylcholinesterase were evaluated. Thirteen alkaloids have been identified among these species, while six unidentified structures have also been detected in these plants. The alkaloid extract of the C. variegatus samples showed the highest structural diversity as well as the best activity against AChE, which was likely due to the presence of the alkaloid sanguinine. The results suggest this genus as a possible interesting new source of Amaryllidaceae alkaloids, which could contribute to the development of new medicines. MDPI 2023-07-14 /pmc/articles/PMC10385320/ /pubmed/37513280 http://dx.doi.org/10.3390/molecules28145408 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rodríguez-Escobar, María Lenny
Tallini, Luciana R.
Lisa-Molina, Julia
Berkov, Strahil
Viladomat, Francesc
Meerow, Alan
Bastida, Jaume
Torras-Claveria, Laura
Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America
title Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America
title_full Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America
title_fullStr Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America
title_full_unstemmed Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America
title_short Chemical and Biological Aspects of Different Species of the Genus Clinanthus Herb. (Amaryllidaceae) from South America
title_sort chemical and biological aspects of different species of the genus clinanthus herb. (amaryllidaceae) from south america
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385320/
https://www.ncbi.nlm.nih.gov/pubmed/37513280
http://dx.doi.org/10.3390/molecules28145408
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