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Ulososides and Urabosides — Triterpenoid Saponins from the Caribbean Marine Sponge Ectyoplasia ferox

Three new triterpene glycosides, named ulososide F (1), urabosides A (2) and B (3), together with the previously reported ulososide A (4), were isolated from the Caribbean marine sponge Ectyoplasia ferox. Their structures were elucidated using extensive interpretation of 1D and 2D-NMR data, as well...

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Autores principales: Colorado, Jhonny, Muñoz, Diana, Marquez, Diana, Marquez, Maria Elena, Lopez, Juan, Thomas, Olivier P., Martinez, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270507/
https://www.ncbi.nlm.nih.gov/pubmed/23446917
http://dx.doi.org/10.3390/molecules18032598
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author Colorado, Jhonny
Muñoz, Diana
Marquez, Diana
Marquez, Maria Elena
Lopez, Juan
Thomas, Olivier P.
Martinez, Alejandro
author_facet Colorado, Jhonny
Muñoz, Diana
Marquez, Diana
Marquez, Maria Elena
Lopez, Juan
Thomas, Olivier P.
Martinez, Alejandro
author_sort Colorado, Jhonny
collection PubMed
description Three new triterpene glycosides, named ulososide F (1), urabosides A (2) and B (3), together with the previously reported ulososide A (4), were isolated from the Caribbean marine sponge Ectyoplasia ferox. Their structures were elucidated using extensive interpretation of 1D and 2D-NMR data, as well as HRESIMS. The aglycon of all compounds is a rare 30-norlonastane and the sugar residues were identified after acid hydrolysis and GC analyses. Cytotoxicities of the isolated compounds were evaluated against Jurkat and CHO cell lines by a MTT in vitro assay as well as a hemolysis assay. Unexpectedly, all these saponin derivatives showed very low activity in our bioassays.
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spelling pubmed-62705072018-12-20 Ulososides and Urabosides — Triterpenoid Saponins from the Caribbean Marine Sponge Ectyoplasia ferox Colorado, Jhonny Muñoz, Diana Marquez, Diana Marquez, Maria Elena Lopez, Juan Thomas, Olivier P. Martinez, Alejandro Molecules Article Three new triterpene glycosides, named ulososide F (1), urabosides A (2) and B (3), together with the previously reported ulososide A (4), were isolated from the Caribbean marine sponge Ectyoplasia ferox. Their structures were elucidated using extensive interpretation of 1D and 2D-NMR data, as well as HRESIMS. The aglycon of all compounds is a rare 30-norlonastane and the sugar residues were identified after acid hydrolysis and GC analyses. Cytotoxicities of the isolated compounds were evaluated against Jurkat and CHO cell lines by a MTT in vitro assay as well as a hemolysis assay. Unexpectedly, all these saponin derivatives showed very low activity in our bioassays. MDPI 2013-02-27 /pmc/articles/PMC6270507/ /pubmed/23446917 http://dx.doi.org/10.3390/molecules18032598 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Colorado, Jhonny
Muñoz, Diana
Marquez, Diana
Marquez, Maria Elena
Lopez, Juan
Thomas, Olivier P.
Martinez, Alejandro
Ulososides and Urabosides — Triterpenoid Saponins from the Caribbean Marine Sponge Ectyoplasia ferox
title Ulososides and Urabosides — Triterpenoid Saponins from the Caribbean Marine Sponge Ectyoplasia ferox
title_full Ulososides and Urabosides — Triterpenoid Saponins from the Caribbean Marine Sponge Ectyoplasia ferox
title_fullStr Ulososides and Urabosides — Triterpenoid Saponins from the Caribbean Marine Sponge Ectyoplasia ferox
title_full_unstemmed Ulososides and Urabosides — Triterpenoid Saponins from the Caribbean Marine Sponge Ectyoplasia ferox
title_short Ulososides and Urabosides — Triterpenoid Saponins from the Caribbean Marine Sponge Ectyoplasia ferox
title_sort ulososides and urabosides — triterpenoid saponins from the caribbean marine sponge ectyoplasia ferox
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270507/
https://www.ncbi.nlm.nih.gov/pubmed/23446917
http://dx.doi.org/10.3390/molecules18032598
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