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Two New Piperazine-Triones from a Marine-Derived Streptomycetes sp. Strain SMS636
Two new piperazine-triones lansai E and F (1, 2), together with four known secondary metabolites lansai D (3), 1-N-methyl-(E,Z)-albonoursin (4), imidazo[4,5-e]-1,2,4-triazine (5), and streptonigrin (6) were isolated from a deep-sea-derived Streptomycetes sp. strain SMS636. The structures of the isol...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471054/ https://www.ncbi.nlm.nih.gov/pubmed/30901830 http://dx.doi.org/10.3390/md17030186 |
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author | Xu, Xiuli Han, Jiahui Lin, Rui Polyak, Steven W. Song, Fuhang |
author_facet | Xu, Xiuli Han, Jiahui Lin, Rui Polyak, Steven W. Song, Fuhang |
author_sort | Xu, Xiuli |
collection | PubMed |
description | Two new piperazine-triones lansai E and F (1, 2), together with four known secondary metabolites lansai D (3), 1-N-methyl-(E,Z)-albonoursin (4), imidazo[4,5-e]-1,2,4-triazine (5), and streptonigrin (6) were isolated from a deep-sea-derived Streptomycetes sp. strain SMS636. The structures of the isolated compounds were confirmed by comprehensive spectroscopic analysis, including HRESIMS, 1D and 2D NMR. Compound 4 exhibited moderate antibacterial activities against Staphylococcus aureus and methicillin resistant S. aureus (MRSA) with Minimum Inhibitory Concentration (MIC) values of 12.5 and 25 μg/mL, respectively. Compound 6 displayed significant antibacterial activities against S. aureus, MRSA and Bacillus Calmette-Guérin (BCG) with MIC values of 0.78, 0.78 and 1.25 μg/mL, respectively. |
format | Online Article Text |
id | pubmed-6471054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64710542019-04-27 Two New Piperazine-Triones from a Marine-Derived Streptomycetes sp. Strain SMS636 Xu, Xiuli Han, Jiahui Lin, Rui Polyak, Steven W. Song, Fuhang Mar Drugs Article Two new piperazine-triones lansai E and F (1, 2), together with four known secondary metabolites lansai D (3), 1-N-methyl-(E,Z)-albonoursin (4), imidazo[4,5-e]-1,2,4-triazine (5), and streptonigrin (6) were isolated from a deep-sea-derived Streptomycetes sp. strain SMS636. The structures of the isolated compounds were confirmed by comprehensive spectroscopic analysis, including HRESIMS, 1D and 2D NMR. Compound 4 exhibited moderate antibacterial activities against Staphylococcus aureus and methicillin resistant S. aureus (MRSA) with Minimum Inhibitory Concentration (MIC) values of 12.5 and 25 μg/mL, respectively. Compound 6 displayed significant antibacterial activities against S. aureus, MRSA and Bacillus Calmette-Guérin (BCG) with MIC values of 0.78, 0.78 and 1.25 μg/mL, respectively. MDPI 2019-03-21 /pmc/articles/PMC6471054/ /pubmed/30901830 http://dx.doi.org/10.3390/md17030186 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Xu, Xiuli Han, Jiahui Lin, Rui Polyak, Steven W. Song, Fuhang Two New Piperazine-Triones from a Marine-Derived Streptomycetes sp. Strain SMS636 |
title | Two New Piperazine-Triones from a Marine-Derived Streptomycetes sp. Strain SMS636 |
title_full | Two New Piperazine-Triones from a Marine-Derived Streptomycetes sp. Strain SMS636 |
title_fullStr | Two New Piperazine-Triones from a Marine-Derived Streptomycetes sp. Strain SMS636 |
title_full_unstemmed | Two New Piperazine-Triones from a Marine-Derived Streptomycetes sp. Strain SMS636 |
title_short | Two New Piperazine-Triones from a Marine-Derived Streptomycetes sp. Strain SMS636 |
title_sort | two new piperazine-triones from a marine-derived streptomycetes sp. strain sms636 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471054/ https://www.ncbi.nlm.nih.gov/pubmed/30901830 http://dx.doi.org/10.3390/md17030186 |
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