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Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus

Sterepinic acids A–C (1–3), new carboxylic acids with two primary alcohols, have been isolated from a fungal strain of Stereum sp. OUPS-124D-1 attached to the marine alga Undaria pinnatifida. Dihydro-1,5-secovibralactone (4), a new vibralactone derivative, was isolated from the same fungal metabolit...

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Autores principales: Yamada, Takeshi, Matsuda, Miwa, Seki, Mayuko, Hirose, Megumi, Kikuchi, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099533/
https://www.ncbi.nlm.nih.gov/pubmed/29865212
http://dx.doi.org/10.3390/molecules23061336
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author Yamada, Takeshi
Matsuda, Miwa
Seki, Mayuko
Hirose, Megumi
Kikuchi, Takashi
author_facet Yamada, Takeshi
Matsuda, Miwa
Seki, Mayuko
Hirose, Megumi
Kikuchi, Takashi
author_sort Yamada, Takeshi
collection PubMed
description Sterepinic acids A–C (1–3), new carboxylic acids with two primary alcohols, have been isolated from a fungal strain of Stereum sp. OUPS-124D-1 attached to the marine alga Undaria pinnatifida. Dihydro-1,5-secovibralactone (4), a new vibralactone derivative, was isolated from the same fungal metabolites together with known vibralactone A (5), and 1,5-secovibralactone (6). The planar structures of these compounds have been elucidated by spectroscopic analyses using IR, HRFABMS, and NMR spectra. To determine the absolute configuration of the compounds, we used the phenylglycine methyl ester (PGME) method. These compounds exhibited less activity in the cytotoxicity assay against cancer cell lines.
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spelling pubmed-60995332018-11-13 Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus Yamada, Takeshi Matsuda, Miwa Seki, Mayuko Hirose, Megumi Kikuchi, Takashi Molecules Article Sterepinic acids A–C (1–3), new carboxylic acids with two primary alcohols, have been isolated from a fungal strain of Stereum sp. OUPS-124D-1 attached to the marine alga Undaria pinnatifida. Dihydro-1,5-secovibralactone (4), a new vibralactone derivative, was isolated from the same fungal metabolites together with known vibralactone A (5), and 1,5-secovibralactone (6). The planar structures of these compounds have been elucidated by spectroscopic analyses using IR, HRFABMS, and NMR spectra. To determine the absolute configuration of the compounds, we used the phenylglycine methyl ester (PGME) method. These compounds exhibited less activity in the cytotoxicity assay against cancer cell lines. MDPI 2018-06-01 /pmc/articles/PMC6099533/ /pubmed/29865212 http://dx.doi.org/10.3390/molecules23061336 Text en © 2018 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yamada, Takeshi
Matsuda, Miwa
Seki, Mayuko
Hirose, Megumi
Kikuchi, Takashi
Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus
title Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus
title_full Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus
title_fullStr Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus
title_full_unstemmed Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus
title_short Sterepinic Acids A–C, New Carboxylic Acids Produced by a Marine Alga-Derived Fungus
title_sort sterepinic acids a–c, new carboxylic acids produced by a marine alga-derived fungus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099533/
https://www.ncbi.nlm.nih.gov/pubmed/29865212
http://dx.doi.org/10.3390/molecules23061336
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