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Briarenones A‒C, New Briarellin Diterpenoids from the Gorgonian Briareum violaceum

Three new eunicellin-derived diterpenoids of briarellin type, briarenones A‒C (1‒3), were isolated from a Formosan gorgonian Briareum violaceum. The chemical structures of the compounds were elucidated on the basis of extensive spectroscopic analyses, including two-dimensional (2D) NMR. The absolute...

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Autores principales: Cheng, Yang, Ahmed, Atallah F., Orfali, Raha S., Dai, Chang-Feng, Sheu, Jyh-Horng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409734/
https://www.ncbi.nlm.nih.gov/pubmed/30781569
http://dx.doi.org/10.3390/md17020120
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author Cheng, Yang
Ahmed, Atallah F.
Orfali, Raha S.
Dai, Chang-Feng
Sheu, Jyh-Horng
author_facet Cheng, Yang
Ahmed, Atallah F.
Orfali, Raha S.
Dai, Chang-Feng
Sheu, Jyh-Horng
author_sort Cheng, Yang
collection PubMed
description Three new eunicellin-derived diterpenoids of briarellin type, briarenones A‒C (1‒3), were isolated from a Formosan gorgonian Briareum violaceum. The chemical structures of the compounds were elucidated on the basis of extensive spectroscopic analyses, including two-dimensional (2D) NMR. The absolute configuration of 1 was further confirmed by a single crystal X-ray diffraction analysis. The in vitro cytotoxic and anti-inflammatory potentialities of the isolated metabolites were tested against the growth of a limited panel of cancer cell lines and against the production of superoxide anions and elastase release in N-formyl-methionyl-leucyl-phenyl-alanine and cytochalasin B (fMLF/CB)-stimulated human neutrophils, respectively.
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spelling pubmed-64097342019-03-29 Briarenones A‒C, New Briarellin Diterpenoids from the Gorgonian Briareum violaceum Cheng, Yang Ahmed, Atallah F. Orfali, Raha S. Dai, Chang-Feng Sheu, Jyh-Horng Mar Drugs Article Three new eunicellin-derived diterpenoids of briarellin type, briarenones A‒C (1‒3), were isolated from a Formosan gorgonian Briareum violaceum. The chemical structures of the compounds were elucidated on the basis of extensive spectroscopic analyses, including two-dimensional (2D) NMR. The absolute configuration of 1 was further confirmed by a single crystal X-ray diffraction analysis. The in vitro cytotoxic and anti-inflammatory potentialities of the isolated metabolites were tested against the growth of a limited panel of cancer cell lines and against the production of superoxide anions and elastase release in N-formyl-methionyl-leucyl-phenyl-alanine and cytochalasin B (fMLF/CB)-stimulated human neutrophils, respectively. MDPI 2019-02-17 /pmc/articles/PMC6409734/ /pubmed/30781569 http://dx.doi.org/10.3390/md17020120 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
Cheng, Yang
Ahmed, Atallah F.
Orfali, Raha S.
Dai, Chang-Feng
Sheu, Jyh-Horng
Briarenones A‒C, New Briarellin Diterpenoids from the Gorgonian Briareum violaceum
title Briarenones A‒C, New Briarellin Diterpenoids from the Gorgonian Briareum violaceum
title_full Briarenones A‒C, New Briarellin Diterpenoids from the Gorgonian Briareum violaceum
title_fullStr Briarenones A‒C, New Briarellin Diterpenoids from the Gorgonian Briareum violaceum
title_full_unstemmed Briarenones A‒C, New Briarellin Diterpenoids from the Gorgonian Briareum violaceum
title_short Briarenones A‒C, New Briarellin Diterpenoids from the Gorgonian Briareum violaceum
title_sort briarenones a‒c, new briarellin diterpenoids from the gorgonian briareum violaceum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409734/
https://www.ncbi.nlm.nih.gov/pubmed/30781569
http://dx.doi.org/10.3390/md17020120
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