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Spiralyde A, an Antikinetoplastid Dolabellane from the Brown Alga Dictyota spiralis

Bioassay-guided fractionation of the antikinetoplastid extract of the brown alga Dictyota spiralis has led to the isolation of spiralyde A (1), a new dolabellane aldehyde, along with other five known related diterpenes (2–6). Their structures were determined by HRESIMS, 1D and 2D NMR spectroscopy, a...

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Autores principales: Chiboub, Olfa, Sifaoui, Ines, Lorenzo-Morales, Jacob, Abderrabba, Manef, Mejri, Mondher, Fernández, José Javier, Piñero, José E., Díaz-Marrero, Ana R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471066/
https://www.ncbi.nlm.nih.gov/pubmed/30934651
http://dx.doi.org/10.3390/md17030192
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author Chiboub, Olfa
Sifaoui, Ines
Lorenzo-Morales, Jacob
Abderrabba, Manef
Mejri, Mondher
Fernández, José Javier
Piñero, José E.
Díaz-Marrero, Ana R.
author_facet Chiboub, Olfa
Sifaoui, Ines
Lorenzo-Morales, Jacob
Abderrabba, Manef
Mejri, Mondher
Fernández, José Javier
Piñero, José E.
Díaz-Marrero, Ana R.
author_sort Chiboub, Olfa
collection PubMed
description Bioassay-guided fractionation of the antikinetoplastid extract of the brown alga Dictyota spiralis has led to the isolation of spiralyde A (1), a new dolabellane aldehyde, along with other five known related diterpenes (2–6). Their structures were determined by HRESIMS, 1D and 2D NMR spectroscopy, and comparison with data reported in the literature. The antiparasitic activity of all compounds was evaluated. Spiralyde A (1) and the known compound 3,4-epoxy-7,18-dolabelladiene (2) were the most active compounds against Leishmania amazonensis and Trypanosoma cruzi. Spiralyde A (1) was the most potent compound, comparable to benznidazole, the reference drug for trypanocidal activity.
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spelling pubmed-64710662019-04-27 Spiralyde A, an Antikinetoplastid Dolabellane from the Brown Alga Dictyota spiralis Chiboub, Olfa Sifaoui, Ines Lorenzo-Morales, Jacob Abderrabba, Manef Mejri, Mondher Fernández, José Javier Piñero, José E. Díaz-Marrero, Ana R. Mar Drugs Article Bioassay-guided fractionation of the antikinetoplastid extract of the brown alga Dictyota spiralis has led to the isolation of spiralyde A (1), a new dolabellane aldehyde, along with other five known related diterpenes (2–6). Their structures were determined by HRESIMS, 1D and 2D NMR spectroscopy, and comparison with data reported in the literature. The antiparasitic activity of all compounds was evaluated. Spiralyde A (1) and the known compound 3,4-epoxy-7,18-dolabelladiene (2) were the most active compounds against Leishmania amazonensis and Trypanosoma cruzi. Spiralyde A (1) was the most potent compound, comparable to benznidazole, the reference drug for trypanocidal activity. MDPI 2019-03-25 /pmc/articles/PMC6471066/ /pubmed/30934651 http://dx.doi.org/10.3390/md17030192 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
Chiboub, Olfa
Sifaoui, Ines
Lorenzo-Morales, Jacob
Abderrabba, Manef
Mejri, Mondher
Fernández, José Javier
Piñero, José E.
Díaz-Marrero, Ana R.
Spiralyde A, an Antikinetoplastid Dolabellane from the Brown Alga Dictyota spiralis
title Spiralyde A, an Antikinetoplastid Dolabellane from the Brown Alga Dictyota spiralis
title_full Spiralyde A, an Antikinetoplastid Dolabellane from the Brown Alga Dictyota spiralis
title_fullStr Spiralyde A, an Antikinetoplastid Dolabellane from the Brown Alga Dictyota spiralis
title_full_unstemmed Spiralyde A, an Antikinetoplastid Dolabellane from the Brown Alga Dictyota spiralis
title_short Spiralyde A, an Antikinetoplastid Dolabellane from the Brown Alga Dictyota spiralis
title_sort spiralyde a, an antikinetoplastid dolabellane from the brown alga dictyota spiralis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471066/
https://www.ncbi.nlm.nih.gov/pubmed/30934651
http://dx.doi.org/10.3390/md17030192
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