Update of Spectroscopic Data for 4-Hydroxydictyolactone and Dictyol E Isolated from a Halimeda stuposa — Dictyota sp. Assemblage (†)

The methanol extract of an assemblage of Halimeda stuposa and a Dictyota sp., yielded three natural products characteristic of Dictyota sp., and one of Halimeda sp. These included the xenicane diterpene 4-hydroxydictyolactone (1), and the diterpenes dictyol E (2), 8α,11-dihydroxypachydictyol A (3) a...

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Detalles Bibliográficos
Autores principales: Ovenden, Simon P. B., Nielson, Jonathan L., Liptrot, Catherine H., Willis, Richard H., Tapiolas, Dianne M., Wright, Anthony D., Motti, Cherie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268996/
https://www.ncbi.nlm.nih.gov/pubmed/22402763
http://dx.doi.org/10.3390/molecules17032929
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author Ovenden, Simon P. B.
Nielson, Jonathan L.
Liptrot, Catherine H.
Willis, Richard H.
Tapiolas, Dianne M.
Wright, Anthony D.
Motti, Cherie A.
author_facet Ovenden, Simon P. B.
Nielson, Jonathan L.
Liptrot, Catherine H.
Willis, Richard H.
Tapiolas, Dianne M.
Wright, Anthony D.
Motti, Cherie A.
author_sort Ovenden, Simon P. B.
collection PubMed
description The methanol extract of an assemblage of Halimeda stuposa and a Dictyota sp., yielded three natural products characteristic of Dictyota sp., and one of Halimeda sp. These included the xenicane diterpene 4-hydroxydictyolactone (1), and the diterpenes dictyol E (2), 8α,11-dihydroxypachydictyol A (3) and indole-3-carboxaldehyde (4). A minor revision of 1 and new spectroscopic data for 1 and 2 are provided, along with associated anti-cancer activities of compounds 1–4.
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spelling pubmed-62689962018-12-20 Update of Spectroscopic Data for 4-Hydroxydictyolactone and Dictyol E Isolated from a Halimeda stuposa — Dictyota sp. Assemblage (†) Ovenden, Simon P. B. Nielson, Jonathan L. Liptrot, Catherine H. Willis, Richard H. Tapiolas, Dianne M. Wright, Anthony D. Motti, Cherie A. Molecules Article The methanol extract of an assemblage of Halimeda stuposa and a Dictyota sp., yielded three natural products characteristic of Dictyota sp., and one of Halimeda sp. These included the xenicane diterpene 4-hydroxydictyolactone (1), and the diterpenes dictyol E (2), 8α,11-dihydroxypachydictyol A (3) and indole-3-carboxaldehyde (4). A minor revision of 1 and new spectroscopic data for 1 and 2 are provided, along with associated anti-cancer activities of compounds 1–4. MDPI 2012-03-08 /pmc/articles/PMC6268996/ /pubmed/22402763 http://dx.doi.org/10.3390/molecules17032929 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
Ovenden, Simon P. B.
Nielson, Jonathan L.
Liptrot, Catherine H.
Willis, Richard H.
Tapiolas, Dianne M.
Wright, Anthony D.
Motti, Cherie A.
Update of Spectroscopic Data for 4-Hydroxydictyolactone and Dictyol E Isolated from a Halimeda stuposa — Dictyota sp. Assemblage (†)
title Update of Spectroscopic Data for 4-Hydroxydictyolactone and Dictyol E Isolated from a Halimeda stuposa — Dictyota sp. Assemblage (†)
title_full Update of Spectroscopic Data for 4-Hydroxydictyolactone and Dictyol E Isolated from a Halimeda stuposa — Dictyota sp. Assemblage (†)
title_fullStr Update of Spectroscopic Data for 4-Hydroxydictyolactone and Dictyol E Isolated from a Halimeda stuposa — Dictyota sp. Assemblage (†)
title_full_unstemmed Update of Spectroscopic Data for 4-Hydroxydictyolactone and Dictyol E Isolated from a Halimeda stuposa — Dictyota sp. Assemblage (†)
title_short Update of Spectroscopic Data for 4-Hydroxydictyolactone and Dictyol E Isolated from a Halimeda stuposa — Dictyota sp. Assemblage (†)
title_sort update of spectroscopic data for 4-hydroxydictyolactone and dictyol e isolated from a halimeda stuposa — dictyota sp. assemblage (†)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268996/
https://www.ncbi.nlm.nih.gov/pubmed/22402763
http://dx.doi.org/10.3390/molecules17032929
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