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New Scabimycins A-C Isolated from Streptomyces acidiscabies (Lu19992)

Peptide natural products displaying a wide range of biological activities have become important drug candidates over the years. Microorganisms have been a powerful source of such bioactive peptides, and Streptomyces have yielded many novel natural products thus far. In an effort to uncover such new,...

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Detalles Bibliográficos
Autores principales: Paulus, Constanze, Zapp, Josef, Luzhetskyy, Andriy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513078/
https://www.ncbi.nlm.nih.gov/pubmed/34641466
http://dx.doi.org/10.3390/molecules26195922
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author Paulus, Constanze
Zapp, Josef
Luzhetskyy, Andriy
author_facet Paulus, Constanze
Zapp, Josef
Luzhetskyy, Andriy
author_sort Paulus, Constanze
collection PubMed
description Peptide natural products displaying a wide range of biological activities have become important drug candidates over the years. Microorganisms have been a powerful source of such bioactive peptides, and Streptomyces have yielded many novel natural products thus far. In an effort to uncover such new, meaningful compounds, the metabolome of Streptomyces acidiscabies was analyzed thoroughly. Three new compounds, scabimycins A–C (1–3), were discovered, and their chemical structures were elucidated by NMR spectroscopy. The relative and absolute configurations were determined using ROESY NMR experiments and advanced Marfey’s method.
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spelling pubmed-85130782021-10-14 New Scabimycins A-C Isolated from Streptomyces acidiscabies (Lu19992) Paulus, Constanze Zapp, Josef Luzhetskyy, Andriy Molecules Article Peptide natural products displaying a wide range of biological activities have become important drug candidates over the years. Microorganisms have been a powerful source of such bioactive peptides, and Streptomyces have yielded many novel natural products thus far. In an effort to uncover such new, meaningful compounds, the metabolome of Streptomyces acidiscabies was analyzed thoroughly. Three new compounds, scabimycins A–C (1–3), were discovered, and their chemical structures were elucidated by NMR spectroscopy. The relative and absolute configurations were determined using ROESY NMR experiments and advanced Marfey’s method. MDPI 2021-09-29 /pmc/articles/PMC8513078/ /pubmed/34641466 http://dx.doi.org/10.3390/molecules26195922 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Paulus, Constanze
Zapp, Josef
Luzhetskyy, Andriy
New Scabimycins A-C Isolated from Streptomyces acidiscabies (Lu19992)
title New Scabimycins A-C Isolated from Streptomyces acidiscabies (Lu19992)
title_full New Scabimycins A-C Isolated from Streptomyces acidiscabies (Lu19992)
title_fullStr New Scabimycins A-C Isolated from Streptomyces acidiscabies (Lu19992)
title_full_unstemmed New Scabimycins A-C Isolated from Streptomyces acidiscabies (Lu19992)
title_short New Scabimycins A-C Isolated from Streptomyces acidiscabies (Lu19992)
title_sort new scabimycins a-c isolated from streptomyces acidiscabies (lu19992)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513078/
https://www.ncbi.nlm.nih.gov/pubmed/34641466
http://dx.doi.org/10.3390/molecules26195922
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