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Nocapyrones: α- and γ-Pyrones from a Marine-Derived Nocardiopsis sp.
One new α-pyrone (nocapyrone R (1)), and three known γ-pyrones (nocapyrones B, H and L (2–4)) were isolated from the culture extract of a Nocardiopsis strain collected from marine sediment. Structures of these compounds were determined on the basis of spectroscopic data including NMR and MS. γ-Pyron...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113818/ https://www.ncbi.nlm.nih.gov/pubmed/25007160 http://dx.doi.org/10.3390/md12074110 |
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author | Kim, Youngju Ogura, Hiromu Akasaka, Kazuaki Oikawa, Tsutomu Matsuura, Nobuyasu Imada, Chiaki Yasuda, Hisato Igarashi, Yasuhiro |
author_facet | Kim, Youngju Ogura, Hiromu Akasaka, Kazuaki Oikawa, Tsutomu Matsuura, Nobuyasu Imada, Chiaki Yasuda, Hisato Igarashi, Yasuhiro |
author_sort | Kim, Youngju |
collection | PubMed |
description | One new α-pyrone (nocapyrone R (1)), and three known γ-pyrones (nocapyrones B, H and L (2–4)) were isolated from the culture extract of a Nocardiopsis strain collected from marine sediment. Structures of these compounds were determined on the basis of spectroscopic data including NMR and MS. γ-Pyrones 2–4 were found to induce adiponectin production in murine ST-13 preadipocyte cells but the α-pyrone 1 had no activity. The absolute configuration of the anteiso-methyl branching in 4 was determined by HPLC comparison of a degraded product of 4 with standard samples as a 2:3 enantiomeric mixture of (R)- and (S)-isomers. |
format | Online Article Text |
id | pubmed-4113818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-41138182014-07-29 Nocapyrones: α- and γ-Pyrones from a Marine-Derived Nocardiopsis sp. Kim, Youngju Ogura, Hiromu Akasaka, Kazuaki Oikawa, Tsutomu Matsuura, Nobuyasu Imada, Chiaki Yasuda, Hisato Igarashi, Yasuhiro Mar Drugs Article One new α-pyrone (nocapyrone R (1)), and three known γ-pyrones (nocapyrones B, H and L (2–4)) were isolated from the culture extract of a Nocardiopsis strain collected from marine sediment. Structures of these compounds were determined on the basis of spectroscopic data including NMR and MS. γ-Pyrones 2–4 were found to induce adiponectin production in murine ST-13 preadipocyte cells but the α-pyrone 1 had no activity. The absolute configuration of the anteiso-methyl branching in 4 was determined by HPLC comparison of a degraded product of 4 with standard samples as a 2:3 enantiomeric mixture of (R)- and (S)-isomers. MDPI 2014-07-08 /pmc/articles/PMC4113818/ /pubmed/25007160 http://dx.doi.org/10.3390/md12074110 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 | Article Kim, Youngju Ogura, Hiromu Akasaka, Kazuaki Oikawa, Tsutomu Matsuura, Nobuyasu Imada, Chiaki Yasuda, Hisato Igarashi, Yasuhiro Nocapyrones: α- and γ-Pyrones from a Marine-Derived Nocardiopsis sp. |
title | Nocapyrones: α- and γ-Pyrones from a Marine-Derived Nocardiopsis sp. |
title_full | Nocapyrones: α- and γ-Pyrones from a Marine-Derived Nocardiopsis sp. |
title_fullStr | Nocapyrones: α- and γ-Pyrones from a Marine-Derived Nocardiopsis sp. |
title_full_unstemmed | Nocapyrones: α- and γ-Pyrones from a Marine-Derived Nocardiopsis sp. |
title_short | Nocapyrones: α- and γ-Pyrones from a Marine-Derived Nocardiopsis sp. |
title_sort | nocapyrones: α- and γ-pyrones from a marine-derived nocardiopsis sp. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113818/ https://www.ncbi.nlm.nih.gov/pubmed/25007160 http://dx.doi.org/10.3390/md12074110 |
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