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New Briarane Diterpenoids from the Gorgonian Coral Junceella juncea
Chemical investigation of Junceella juncea has resulted in the isolation of three new briaranes designated juncenolides M–O (1–3). The structures of these compounds were determined by spectroscopic analysis including 2D-NMR (COSY, HMBC and NOESY) and HRMS. Compound 1 is a new chlorinated briarane wh...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397442/ https://www.ncbi.nlm.nih.gov/pubmed/22822375 http://dx.doi.org/10.3390/md10061321 |
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author | Chang, Jiun-Yang Liaw, Chia-Ching Fazary, Ahmed Eid Hwang, Tsong-Long Shen, Ya-Ching |
author_facet | Chang, Jiun-Yang Liaw, Chia-Ching Fazary, Ahmed Eid Hwang, Tsong-Long Shen, Ya-Ching |
author_sort | Chang, Jiun-Yang |
collection | PubMed |
description | Chemical investigation of Junceella juncea has resulted in the isolation of three new briaranes designated juncenolides M–O (1–3). The structures of these compounds were determined by spectroscopic analysis including 2D-NMR (COSY, HMBC and NOESY) and HRMS. Compound 1 is a new chlorinated briarane while compound 3 contains a rare methyl ester at C-16. The anti-inflammatory activities tested on superoxide anion generation and elastase release by human neutrophils in response to FMLP/CB were evaluated. |
format | Online Article Text |
id | pubmed-3397442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-33974422012-07-20 New Briarane Diterpenoids from the Gorgonian Coral Junceella juncea Chang, Jiun-Yang Liaw, Chia-Ching Fazary, Ahmed Eid Hwang, Tsong-Long Shen, Ya-Ching Mar Drugs Article Chemical investigation of Junceella juncea has resulted in the isolation of three new briaranes designated juncenolides M–O (1–3). The structures of these compounds were determined by spectroscopic analysis including 2D-NMR (COSY, HMBC and NOESY) and HRMS. Compound 1 is a new chlorinated briarane while compound 3 contains a rare methyl ester at C-16. The anti-inflammatory activities tested on superoxide anion generation and elastase release by human neutrophils in response to FMLP/CB were evaluated. MDPI 2012-06-07 /pmc/articles/PMC3397442/ /pubmed/22822375 http://dx.doi.org/10.3390/md10061321 Text en © 2012 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 Chang, Jiun-Yang Liaw, Chia-Ching Fazary, Ahmed Eid Hwang, Tsong-Long Shen, Ya-Ching New Briarane Diterpenoids from the Gorgonian Coral Junceella juncea |
title | New Briarane Diterpenoids from the Gorgonian Coral Junceella juncea |
title_full | New Briarane Diterpenoids from the Gorgonian Coral Junceella juncea |
title_fullStr | New Briarane Diterpenoids from the Gorgonian Coral Junceella juncea |
title_full_unstemmed | New Briarane Diterpenoids from the Gorgonian Coral Junceella juncea |
title_short | New Briarane Diterpenoids from the Gorgonian Coral Junceella juncea |
title_sort | new briarane diterpenoids from the gorgonian coral junceella juncea |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397442/ https://www.ncbi.nlm.nih.gov/pubmed/22822375 http://dx.doi.org/10.3390/md10061321 |
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