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New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum

Four new sulfated sesquiterpene hydroquinones siphonodictyals E1–E4 (1–4) and cyclosiphonodictyol A (5) were isolated from a sample of the Caribbean sponge Aka coralliphagum collected off the coast of San Salvador in the Bahamas. The structures of the new compounds were elucidated on the basis of ma...

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Autores principales: Göthel, Qun, Köck, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999825/
https://www.ncbi.nlm.nih.gov/pubmed/24778711
http://dx.doi.org/10.3762/bjoc.10.52
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author Göthel, Qun
Köck, Matthias
author_facet Göthel, Qun
Köck, Matthias
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collection PubMed
description Four new sulfated sesquiterpene hydroquinones siphonodictyals E1–E4 (1–4) and cyclosiphonodictyol A (5) were isolated from a sample of the Caribbean sponge Aka coralliphagum collected off the coast of San Salvador in the Bahamas. The structures of the new compounds were elucidated on the basis of mass spectrometric and NMR spectroscopic analysis. Compounds 1–4 are derivatives of siphonodictyal E (9). Siphonodictyal E4 (4) exhibited mild antiproliferation activity against L929 mouse fibroblast, KB-31 epidermoid carcinoma, and MCF-7 breast cancer cell lines, while siphondictyal E3 (3) and cyclosiphonodictyol A (5) showed moderate activity against Gram-positive bacteria.
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spelling pubmed-39998252014-04-28 New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum Göthel, Qun Köck, Matthias Beilstein J Org Chem Full Research Paper Four new sulfated sesquiterpene hydroquinones siphonodictyals E1–E4 (1–4) and cyclosiphonodictyol A (5) were isolated from a sample of the Caribbean sponge Aka coralliphagum collected off the coast of San Salvador in the Bahamas. The structures of the new compounds were elucidated on the basis of mass spectrometric and NMR spectroscopic analysis. Compounds 1–4 are derivatives of siphonodictyal E (9). Siphonodictyal E4 (4) exhibited mild antiproliferation activity against L929 mouse fibroblast, KB-31 epidermoid carcinoma, and MCF-7 breast cancer cell lines, while siphondictyal E3 (3) and cyclosiphonodictyol A (5) showed moderate activity against Gram-positive bacteria. Beilstein-Institut 2014-03-06 /pmc/articles/PMC3999825/ /pubmed/24778711 http://dx.doi.org/10.3762/bjoc.10.52 Text en Copyright © 2014, Göthel and Köck https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Göthel, Qun
Köck, Matthias
New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum
title New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum
title_full New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum
title_fullStr New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum
title_full_unstemmed New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum
title_short New sesquiterpene hydroquinones from the Caribbean sponge Aka coralliphagum
title_sort new sesquiterpene hydroquinones from the caribbean sponge aka coralliphagum
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999825/
https://www.ncbi.nlm.nih.gov/pubmed/24778711
http://dx.doi.org/10.3762/bjoc.10.52
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