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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...

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Autores principales: Kim, Youngju, Ogura, Hiromu, Akasaka, Kazuaki, Oikawa, Tsutomu, Matsuura, Nobuyasu, Imada, Chiaki, Yasuda, Hisato, Igarashi, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
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.
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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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