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New azaphilones from Aspergillus neoglaber

Three new azaphilones, sassafrin E (1), sassafrin F (2), and sassafrinamine A (3), were isolated from the filamentous fungus Aspergillus neoglaber. The structures of the compounds were determined by nuclear magnetic resonance spectroscopy, and were found to be novel analogues of two already known co...

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Autores principales: Isbrandt, Thomas, Frisvad, Jens C., Madsen, Anja, Larsen, Thomas O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431503/
https://www.ncbi.nlm.nih.gov/pubmed/32804338
http://dx.doi.org/10.1186/s13568-020-01078-4
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author Isbrandt, Thomas
Frisvad, Jens C.
Madsen, Anja
Larsen, Thomas O.
author_facet Isbrandt, Thomas
Frisvad, Jens C.
Madsen, Anja
Larsen, Thomas O.
author_sort Isbrandt, Thomas
collection PubMed
description Three new azaphilones, sassafrin E (1), sassafrin F (2), and sassafrinamine A (3), were isolated from the filamentous fungus Aspergillus neoglaber. The structures of the compounds were determined by nuclear magnetic resonance spectroscopy, and were found to be novel analogues of two already known compound classes; sassafrins and berkchaetoazaphilones. Sassafrin E and F were both oxygen containing, while sassafrinamine A additionally contained a nitrogen atom, originating from an aminoethanol moiety, as well as extensive conjugation resulting in an intense purple colour of the pure compound. The structure of sassafrin E was further confirmed using deuterium exchange experiments coupled with high-resolution tandem mass spectrometry.
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spelling pubmed-74315032020-08-20 New azaphilones from Aspergillus neoglaber Isbrandt, Thomas Frisvad, Jens C. Madsen, Anja Larsen, Thomas O. AMB Express Original Article Three new azaphilones, sassafrin E (1), sassafrin F (2), and sassafrinamine A (3), were isolated from the filamentous fungus Aspergillus neoglaber. The structures of the compounds were determined by nuclear magnetic resonance spectroscopy, and were found to be novel analogues of two already known compound classes; sassafrins and berkchaetoazaphilones. Sassafrin E and F were both oxygen containing, while sassafrinamine A additionally contained a nitrogen atom, originating from an aminoethanol moiety, as well as extensive conjugation resulting in an intense purple colour of the pure compound. The structure of sassafrin E was further confirmed using deuterium exchange experiments coupled with high-resolution tandem mass spectrometry. Springer Berlin Heidelberg 2020-08-17 /pmc/articles/PMC7431503/ /pubmed/32804338 http://dx.doi.org/10.1186/s13568-020-01078-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Isbrandt, Thomas
Frisvad, Jens C.
Madsen, Anja
Larsen, Thomas O.
New azaphilones from Aspergillus neoglaber
title New azaphilones from Aspergillus neoglaber
title_full New azaphilones from Aspergillus neoglaber
title_fullStr New azaphilones from Aspergillus neoglaber
title_full_unstemmed New azaphilones from Aspergillus neoglaber
title_short New azaphilones from Aspergillus neoglaber
title_sort new azaphilones from aspergillus neoglaber
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431503/
https://www.ncbi.nlm.nih.gov/pubmed/32804338
http://dx.doi.org/10.1186/s13568-020-01078-4
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