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Monasnicotinates A–D, Four New Pyridine Alkaloids from the Fungal Strain Monascus pilosus BCRC 38093
Four new pyridine derivatives, monasnicotinates A–D (1–4) were isolated from the red yeast rice of Monascus pilosus BCRC 38093. Their structures were elucidated on the basis of physicochemical evidence, in-depth NMR spectroscopic analysis, and high-resolution mass spectrometry. Their inhibitory effe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264138/ https://www.ncbi.nlm.nih.gov/pubmed/21654578 http://dx.doi.org/10.3390/molecules16064719 |
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author | Wu, Ming-Der Cheng, Ming-Jen Yech, Yi-Jen Chen, Yen-Lin Chen, Kai-Ping Chen, Ih-Sheng Yang, Ping-Hsun Yuan, Gwo-Fang |
author_facet | Wu, Ming-Der Cheng, Ming-Jen Yech, Yi-Jen Chen, Yen-Lin Chen, Kai-Ping Chen, Ih-Sheng Yang, Ping-Hsun Yuan, Gwo-Fang |
author_sort | Wu, Ming-Der |
collection | PubMed |
description | Four new pyridine derivatives, monasnicotinates A–D (1–4) were isolated from the red yeast rice of Monascus pilosus BCRC 38093. Their structures were elucidated on the basis of physicochemical evidence, in-depth NMR spectroscopic analysis, and high-resolution mass spectrometry. Their inhibitory effects on NO production was also evaluated. |
format | Online Article Text |
id | pubmed-6264138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62641382018-12-10 Monasnicotinates A–D, Four New Pyridine Alkaloids from the Fungal Strain Monascus pilosus BCRC 38093 Wu, Ming-Der Cheng, Ming-Jen Yech, Yi-Jen Chen, Yen-Lin Chen, Kai-Ping Chen, Ih-Sheng Yang, Ping-Hsun Yuan, Gwo-Fang Molecules Article Four new pyridine derivatives, monasnicotinates A–D (1–4) were isolated from the red yeast rice of Monascus pilosus BCRC 38093. Their structures were elucidated on the basis of physicochemical evidence, in-depth NMR spectroscopic analysis, and high-resolution mass spectrometry. Their inhibitory effects on NO production was also evaluated. MDPI 2011-06-07 /pmc/articles/PMC6264138/ /pubmed/21654578 http://dx.doi.org/10.3390/molecules16064719 Text en © 2011 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 Wu, Ming-Der Cheng, Ming-Jen Yech, Yi-Jen Chen, Yen-Lin Chen, Kai-Ping Chen, Ih-Sheng Yang, Ping-Hsun Yuan, Gwo-Fang Monasnicotinates A–D, Four New Pyridine Alkaloids from the Fungal Strain Monascus pilosus BCRC 38093 |
title | Monasnicotinates A–D, Four New Pyridine Alkaloids from the Fungal Strain Monascus pilosus BCRC 38093 |
title_full | Monasnicotinates A–D, Four New Pyridine Alkaloids from the Fungal Strain Monascus pilosus BCRC 38093 |
title_fullStr | Monasnicotinates A–D, Four New Pyridine Alkaloids from the Fungal Strain Monascus pilosus BCRC 38093 |
title_full_unstemmed | Monasnicotinates A–D, Four New Pyridine Alkaloids from the Fungal Strain Monascus pilosus BCRC 38093 |
title_short | Monasnicotinates A–D, Four New Pyridine Alkaloids from the Fungal Strain Monascus pilosus BCRC 38093 |
title_sort | monasnicotinates a–d, four new pyridine alkaloids from the fungal strain monascus pilosus bcrc 38093 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264138/ https://www.ncbi.nlm.nih.gov/pubmed/21654578 http://dx.doi.org/10.3390/molecules16064719 |
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