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Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans

Four new sesquiterpene hydroquinones, xishaeleganins A–D (6–9), along with eleven known related ones (12 and 14–23) were isolated from the Xisha marine sponge Dactylospongia elegans (family Thorectida). Their structures were determined by extensive spectroscopic analysis, ECD calculations, and by co...

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Autores principales: Chen, Bao, Zhao, Qingmin, Gu, Yu-Cheng, Lan, Lefu, Wang, Chang-Yun, Guo, Yue-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879793/
https://www.ncbi.nlm.nih.gov/pubmed/35200647
http://dx.doi.org/10.3390/md20020118
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author Chen, Bao
Zhao, Qingmin
Gu, Yu-Cheng
Lan, Lefu
Wang, Chang-Yun
Guo, Yue-Wei
author_facet Chen, Bao
Zhao, Qingmin
Gu, Yu-Cheng
Lan, Lefu
Wang, Chang-Yun
Guo, Yue-Wei
author_sort Chen, Bao
collection PubMed
description Four new sesquiterpene hydroquinones, xishaeleganins A–D (6–9), along with eleven known related ones (12 and 14–23) were isolated from the Xisha marine sponge Dactylospongia elegans (family Thorectida). Their structures were determined by extensive spectroscopic analysis, ECD calculations, and by comparison with the spectral data reported in the literature. Compounds 7, 15, 20, and 21 showed significant antibacterial activity against Staphylococcus aureus, with minimum inhibitory concentration values of 1.5, 2.9, 5.6, and 5.6 µg/mL, which are comparable with those obtained for the positive control vancomycin (MIC: 1.0 µg/mL).
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spelling pubmed-88797932022-02-26 Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans Chen, Bao Zhao, Qingmin Gu, Yu-Cheng Lan, Lefu Wang, Chang-Yun Guo, Yue-Wei Mar Drugs Article Four new sesquiterpene hydroquinones, xishaeleganins A–D (6–9), along with eleven known related ones (12 and 14–23) were isolated from the Xisha marine sponge Dactylospongia elegans (family Thorectida). Their structures were determined by extensive spectroscopic analysis, ECD calculations, and by comparison with the spectral data reported in the literature. Compounds 7, 15, 20, and 21 showed significant antibacterial activity against Staphylococcus aureus, with minimum inhibitory concentration values of 1.5, 2.9, 5.6, and 5.6 µg/mL, which are comparable with those obtained for the positive control vancomycin (MIC: 1.0 µg/mL). MDPI 2022-02-01 /pmc/articles/PMC8879793/ /pubmed/35200647 http://dx.doi.org/10.3390/md20020118 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Bao
Zhao, Qingmin
Gu, Yu-Cheng
Lan, Lefu
Wang, Chang-Yun
Guo, Yue-Wei
Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans
title Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans
title_full Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans
title_fullStr Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans
title_full_unstemmed Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans
title_short Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans
title_sort xishaeleganins a–d, sesquiterpenoid hydroquinones from xisha marine sponge dactylospongia elegans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879793/
https://www.ncbi.nlm.nih.gov/pubmed/35200647
http://dx.doi.org/10.3390/md20020118
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