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Mode of Action of Diterpene and Characterization of Related Metabolites from the Soft Coral, Xenia elongata

Chemical and biological investigation of the cultured marine soft coral Xenia elongata led to the isolation of two new diterpenes (2, 3). Their structures were elucidated using a combination of NMR and mass spectrometry. Biological evaluations and assessments were determined using the specific apopt...

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Autores principales: Andrianasolo, Eric H., Haramaty, Liti, White, Eileen, Lutz, Richard, Falkowski, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944532/
https://www.ncbi.nlm.nih.gov/pubmed/24562393
http://dx.doi.org/10.3390/md12021102
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author Andrianasolo, Eric H.
Haramaty, Liti
White, Eileen
Lutz, Richard
Falkowski, Paul
author_facet Andrianasolo, Eric H.
Haramaty, Liti
White, Eileen
Lutz, Richard
Falkowski, Paul
author_sort Andrianasolo, Eric H.
collection PubMed
description Chemical and biological investigation of the cultured marine soft coral Xenia elongata led to the isolation of two new diterpenes (2, 3). Their structures were elucidated using a combination of NMR and mass spectrometry. Biological evaluations and assessments were determined using the specific apoptosis induction assay based on genetically engineered mammalian cell line D3 deficient in Bak and Bax and derived from a mouse epithelial cell. The diterpenes induce apoptosis in low micromolar concentrations. The results indicate that the previously isolated compound (1) affects cell in a manner similar to that of HSP90 and HDAC inhibitors and in a manner opposite of PI3 kinase/mTOR inhibitors. Compound (3) inhibits selectively HDAC6 in high micromolar concentrations.
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spelling pubmed-39445322014-03-07 Mode of Action of Diterpene and Characterization of Related Metabolites from the Soft Coral, Xenia elongata Andrianasolo, Eric H. Haramaty, Liti White, Eileen Lutz, Richard Falkowski, Paul Mar Drugs Chemical and biological investigation of the cultured marine soft coral Xenia elongata led to the isolation of two new diterpenes (2, 3). Their structures were elucidated using a combination of NMR and mass spectrometry. Biological evaluations and assessments were determined using the specific apoptosis induction assay based on genetically engineered mammalian cell line D3 deficient in Bak and Bax and derived from a mouse epithelial cell. The diterpenes induce apoptosis in low micromolar concentrations. The results indicate that the previously isolated compound (1) affects cell in a manner similar to that of HSP90 and HDAC inhibitors and in a manner opposite of PI3 kinase/mTOR inhibitors. Compound (3) inhibits selectively HDAC6 in high micromolar concentrations. MDPI 2014-02-20 /pmc/articles/PMC3944532/ /pubmed/24562393 http://dx.doi.org/10.3390/md12021102 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 Andrianasolo, Eric H.
Haramaty, Liti
White, Eileen
Lutz, Richard
Falkowski, Paul
Mode of Action of Diterpene and Characterization of Related Metabolites from the Soft Coral, Xenia elongata
title Mode of Action of Diterpene and Characterization of Related Metabolites from the Soft Coral, Xenia elongata
title_full Mode of Action of Diterpene and Characterization of Related Metabolites from the Soft Coral, Xenia elongata
title_fullStr Mode of Action of Diterpene and Characterization of Related Metabolites from the Soft Coral, Xenia elongata
title_full_unstemmed Mode of Action of Diterpene and Characterization of Related Metabolites from the Soft Coral, Xenia elongata
title_short Mode of Action of Diterpene and Characterization of Related Metabolites from the Soft Coral, Xenia elongata
title_sort mode of action of diterpene and characterization of related metabolites from the soft coral, xenia elongata
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944532/
https://www.ncbi.nlm.nih.gov/pubmed/24562393
http://dx.doi.org/10.3390/md12021102
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