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Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis
Sesquiterpene lactones are naturally occurring compounds mainly found in the Asteraceae family. These types of plant metabolites display a wide range of biological activities, including antiprotozoal activity and are considered interesting structures for drug discovery. Four derivatives were synthes...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479983/ https://www.ncbi.nlm.nih.gov/pubmed/30925657 http://dx.doi.org/10.3390/molecules24071209 |
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author | Sülsen, Valeria P. Lizarraga, Emilio F. Elso, Orlando G. Cerny, Natacha Sanchez Alberti, Andrés Bivona, Augusto E. Malchiodi, Emilio L. Cazorla, Silvia I. Catalán, César A. N. |
author_facet | Sülsen, Valeria P. Lizarraga, Emilio F. Elso, Orlando G. Cerny, Natacha Sanchez Alberti, Andrés Bivona, Augusto E. Malchiodi, Emilio L. Cazorla, Silvia I. Catalán, César A. N. |
author_sort | Sülsen, Valeria P. |
collection | PubMed |
description | Sesquiterpene lactones are naturally occurring compounds mainly found in the Asteraceae family. These types of plant metabolites display a wide range of biological activities, including antiprotozoal activity and are considered interesting structures for drug discovery. Four derivatives were synthesized from estafietin (1), isolated from Stevia alpina (Asteraceae): 11βH,13-dihydroestafietin (2), epoxyestafietin (3a and 3b), 11βH,13-methoxyestafietin, (4) and 11βH,13-cianoestafietin. The antiprotozoal activity against Trypanosoma cruzi and Leishmania braziliensis of these compounds was evaluated. Epoxyestafietin was the most active compound against T. cruzi trypomastigotes and amastigotes (IC(50) values of 18.7 and 2.0 µg/mL, respectively). Estafietin (1) and 11βH,13-dihydroestafietin (2) were the most active and selective compounds on L. braziliensis promastigotes (IC(50) values of 1.0 and 1.3 μg/mL, respectively). The antiparasitic activity demonstrated by estafietin and some of its derivatives make them promising candidates for the development of effective compounds for the treatment of Chagas disease and leihsmaniasis. |
format | Online Article Text |
id | pubmed-6479983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64799832019-04-30 Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis Sülsen, Valeria P. Lizarraga, Emilio F. Elso, Orlando G. Cerny, Natacha Sanchez Alberti, Andrés Bivona, Augusto E. Malchiodi, Emilio L. Cazorla, Silvia I. Catalán, César A. N. Molecules Article Sesquiterpene lactones are naturally occurring compounds mainly found in the Asteraceae family. These types of plant metabolites display a wide range of biological activities, including antiprotozoal activity and are considered interesting structures for drug discovery. Four derivatives were synthesized from estafietin (1), isolated from Stevia alpina (Asteraceae): 11βH,13-dihydroestafietin (2), epoxyestafietin (3a and 3b), 11βH,13-methoxyestafietin, (4) and 11βH,13-cianoestafietin. The antiprotozoal activity against Trypanosoma cruzi and Leishmania braziliensis of these compounds was evaluated. Epoxyestafietin was the most active compound against T. cruzi trypomastigotes and amastigotes (IC(50) values of 18.7 and 2.0 µg/mL, respectively). Estafietin (1) and 11βH,13-dihydroestafietin (2) were the most active and selective compounds on L. braziliensis promastigotes (IC(50) values of 1.0 and 1.3 μg/mL, respectively). The antiparasitic activity demonstrated by estafietin and some of its derivatives make them promising candidates for the development of effective compounds for the treatment of Chagas disease and leihsmaniasis. MDPI 2019-03-28 /pmc/articles/PMC6479983/ /pubmed/30925657 http://dx.doi.org/10.3390/molecules24071209 Text en © 2019 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 Sülsen, Valeria P. Lizarraga, Emilio F. Elso, Orlando G. Cerny, Natacha Sanchez Alberti, Andrés Bivona, Augusto E. Malchiodi, Emilio L. Cazorla, Silvia I. Catalán, César A. N. Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis |
title | Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis |
title_full | Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis |
title_fullStr | Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis |
title_full_unstemmed | Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis |
title_short | Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis |
title_sort | activity of estafietin and analogues on trypanosoma cruzi and leishmania braziliensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479983/ https://www.ncbi.nlm.nih.gov/pubmed/30925657 http://dx.doi.org/10.3390/molecules24071209 |
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