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Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum
Five new pregnane-type steroids, sclerosteroids J–N (1–5), and a diterpenoid with a new chemotype 3-methyl-5-(10′-acetoxy-2′,6′,10′-trimethylundecyl)-2-penten-5-olide (6), have been isolated from a soft coral Scleronephthya gracillimum. The structures of the metabolites were determined by extensive...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721209/ https://www.ncbi.nlm.nih.gov/pubmed/23760015 http://dx.doi.org/10.3390/md11061853 |
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author | Fang, Hui-Yu Hsu, Chi-Hsin Chao, Chih-Hua Wen, Zhi-Hong Wu, Yang-Chang Dai, Chang-Feng Sheu, Jyh-Horng |
author_facet | Fang, Hui-Yu Hsu, Chi-Hsin Chao, Chih-Hua Wen, Zhi-Hong Wu, Yang-Chang Dai, Chang-Feng Sheu, Jyh-Horng |
author_sort | Fang, Hui-Yu |
collection | PubMed |
description | Five new pregnane-type steroids, sclerosteroids J–N (1–5), and a diterpenoid with a new chemotype 3-methyl-5-(10′-acetoxy-2′,6′,10′-trimethylundecyl)-2-penten-5-olide (6), have been isolated from a soft coral Scleronephthya gracillimum. The structures of the metabolites were determined by extensive spectroscopic analysis. Compound 4 exhibited cytotoxicity against HepG2, A549, and MDA-MB-231 cancer cell lines. Furthermore, steroids 2 and 4 were found to significantly inhibit the accumulation of the pro-inflammatory iNOS protein, and 1, 2, 4 and 5 could effectively reduce the accumulation of COX-2 protein in LPS-stimulated RAW264.7 macrophage cells. |
format | Online Article Text |
id | pubmed-3721209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-37212092013-07-24 Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum Fang, Hui-Yu Hsu, Chi-Hsin Chao, Chih-Hua Wen, Zhi-Hong Wu, Yang-Chang Dai, Chang-Feng Sheu, Jyh-Horng Mar Drugs Article Five new pregnane-type steroids, sclerosteroids J–N (1–5), and a diterpenoid with a new chemotype 3-methyl-5-(10′-acetoxy-2′,6′,10′-trimethylundecyl)-2-penten-5-olide (6), have been isolated from a soft coral Scleronephthya gracillimum. The structures of the metabolites were determined by extensive spectroscopic analysis. Compound 4 exhibited cytotoxicity against HepG2, A549, and MDA-MB-231 cancer cell lines. Furthermore, steroids 2 and 4 were found to significantly inhibit the accumulation of the pro-inflammatory iNOS protein, and 1, 2, 4 and 5 could effectively reduce the accumulation of COX-2 protein in LPS-stimulated RAW264.7 macrophage cells. MDPI 2013-05-29 /pmc/articles/PMC3721209/ /pubmed/23760015 http://dx.doi.org/10.3390/md11061853 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 Fang, Hui-Yu Hsu, Chi-Hsin Chao, Chih-Hua Wen, Zhi-Hong Wu, Yang-Chang Dai, Chang-Feng Sheu, Jyh-Horng Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum |
title | Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum |
title_full | Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum |
title_fullStr | Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum |
title_full_unstemmed | Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum |
title_short | Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum |
title_sort | cytotoxic and anti-inflammatory metabolites from the soft coral scleronephthya gracillimum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721209/ https://www.ncbi.nlm.nih.gov/pubmed/23760015 http://dx.doi.org/10.3390/md11061853 |
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