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Bioactive Cembranoids, Sarcocrassocolides P–R, from the Dongsha Atoll Soft Coral Sarcophyton crassocaule

New cembranoids, sarcocrassocolides P–R (1–3) and four known compounds (4–7) were isolated from the soft coral Sarcophyton crassocaule. The structures of the metabolites were determined by extensive spectroscopic analysis. Compounds 3–5 and 7 were shown to exhibit cytotoxicity toward a limited panel...

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Autores principales: Lin, Wan-Yu, Chen, Bo-Wei, Huang, Chiung-Yao, Wen, Zhi-Hong, Sung, Ping-Jyun, Su, Jui-Hsin, Dai, Chang-Feng, Sheu, Jyh-Horng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944518/
https://www.ncbi.nlm.nih.gov/pubmed/24477285
http://dx.doi.org/10.3390/md12020840
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author Lin, Wan-Yu
Chen, Bo-Wei
Huang, Chiung-Yao
Wen, Zhi-Hong
Sung, Ping-Jyun
Su, Jui-Hsin
Dai, Chang-Feng
Sheu, Jyh-Horng
author_facet Lin, Wan-Yu
Chen, Bo-Wei
Huang, Chiung-Yao
Wen, Zhi-Hong
Sung, Ping-Jyun
Su, Jui-Hsin
Dai, Chang-Feng
Sheu, Jyh-Horng
author_sort Lin, Wan-Yu
collection PubMed
description New cembranoids, sarcocrassocolides P–R (1–3) and four known compounds (4–7) were isolated from the soft coral Sarcophyton crassocaule. The structures of the metabolites were determined by extensive spectroscopic analysis. Compounds 3–5 and 7 were shown to exhibit cytotoxicity toward a limited panel of cancer cell lines and all compounds 1–7 displayed potent in vitro anti-inflammatory activity in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophage cells by inhibiting the expression of inducible nitric oxide synthase (iNOS) protein. Compound 7 also showed significant activity in reducing the accumulation of cyclooxygenase-2 (COX-2) protein in the same macrophage cells.
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spelling pubmed-39445182014-03-07 Bioactive Cembranoids, Sarcocrassocolides P–R, from the Dongsha Atoll Soft Coral Sarcophyton crassocaule Lin, Wan-Yu Chen, Bo-Wei Huang, Chiung-Yao Wen, Zhi-Hong Sung, Ping-Jyun Su, Jui-Hsin Dai, Chang-Feng Sheu, Jyh-Horng Mar Drugs New cembranoids, sarcocrassocolides P–R (1–3) and four known compounds (4–7) were isolated from the soft coral Sarcophyton crassocaule. The structures of the metabolites were determined by extensive spectroscopic analysis. Compounds 3–5 and 7 were shown to exhibit cytotoxicity toward a limited panel of cancer cell lines and all compounds 1–7 displayed potent in vitro anti-inflammatory activity in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophage cells by inhibiting the expression of inducible nitric oxide synthase (iNOS) protein. Compound 7 also showed significant activity in reducing the accumulation of cyclooxygenase-2 (COX-2) protein in the same macrophage cells. MDPI 2014-01-28 /pmc/articles/PMC3944518/ /pubmed/24477285 http://dx.doi.org/10.3390/md12020840 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Lin, Wan-Yu
Chen, Bo-Wei
Huang, Chiung-Yao
Wen, Zhi-Hong
Sung, Ping-Jyun
Su, Jui-Hsin
Dai, Chang-Feng
Sheu, Jyh-Horng
Bioactive Cembranoids, Sarcocrassocolides P–R, from the Dongsha Atoll Soft Coral Sarcophyton crassocaule
title Bioactive Cembranoids, Sarcocrassocolides P–R, from the Dongsha Atoll Soft Coral Sarcophyton crassocaule
title_full Bioactive Cembranoids, Sarcocrassocolides P–R, from the Dongsha Atoll Soft Coral Sarcophyton crassocaule
title_fullStr Bioactive Cembranoids, Sarcocrassocolides P–R, from the Dongsha Atoll Soft Coral Sarcophyton crassocaule
title_full_unstemmed Bioactive Cembranoids, Sarcocrassocolides P–R, from the Dongsha Atoll Soft Coral Sarcophyton crassocaule
title_short Bioactive Cembranoids, Sarcocrassocolides P–R, from the Dongsha Atoll Soft Coral Sarcophyton crassocaule
title_sort bioactive cembranoids, sarcocrassocolides p–r, from the dongsha atoll soft coral sarcophyton crassocaule
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944518/
https://www.ncbi.nlm.nih.gov/pubmed/24477285
http://dx.doi.org/10.3390/md12020840
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