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Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY
Chemical investigation of the cultures of marine Streptomyces sp. 182SMLY led to the discovery of two new polycyclic anthraquinones, which were elucidated as N-acetyl-N-demethylmayamycin (1) and streptoanthraquinone A (2) based on the extensive spectroscopic analysis including 2D NMR, HRESIMS, and a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728507/ https://www.ncbi.nlm.nih.gov/pubmed/26751456 http://dx.doi.org/10.3390/md14010010 |
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author | Liang, Ying Xie, Xin Chen, Lu Yan, Shilun Ye, Xuewei Anjum, Komal Huang, Haocai Lian, Xiaoyuan Zhang, Zhizhen |
author_facet | Liang, Ying Xie, Xin Chen, Lu Yan, Shilun Ye, Xuewei Anjum, Komal Huang, Haocai Lian, Xiaoyuan Zhang, Zhizhen |
author_sort | Liang, Ying |
collection | PubMed |
description | Chemical investigation of the cultures of marine Streptomyces sp. 182SMLY led to the discovery of two new polycyclic anthraquinones, which were elucidated as N-acetyl-N-demethylmayamycin (1) and streptoanthraquinone A (2) based on the extensive spectroscopic analysis including 2D NMR, HRESIMS, and an electronic circular dichroism (ECD) calculation. Both anthraquinones remarkably suppressed the proliferation of four different glioma cell lines with IC(50) values in a range from 0.5 to 7.3 μM and induced apoptosis in the glioma cells. The ratios of IC(50) for normal human astrocytes to IC(50) for glioma cells were 6.4–53 for 1 and >14–31 for 2. N-acetyl-N-demethylmayamycin (1) also inhibited the growth of methicillin-resistant Staphylococcus aureus with MIC 20.0 μM. |
format | Online Article Text |
id | pubmed-4728507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-47285072016-02-08 Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY Liang, Ying Xie, Xin Chen, Lu Yan, Shilun Ye, Xuewei Anjum, Komal Huang, Haocai Lian, Xiaoyuan Zhang, Zhizhen Mar Drugs Article Chemical investigation of the cultures of marine Streptomyces sp. 182SMLY led to the discovery of two new polycyclic anthraquinones, which were elucidated as N-acetyl-N-demethylmayamycin (1) and streptoanthraquinone A (2) based on the extensive spectroscopic analysis including 2D NMR, HRESIMS, and an electronic circular dichroism (ECD) calculation. Both anthraquinones remarkably suppressed the proliferation of four different glioma cell lines with IC(50) values in a range from 0.5 to 7.3 μM and induced apoptosis in the glioma cells. The ratios of IC(50) for normal human astrocytes to IC(50) for glioma cells were 6.4–53 for 1 and >14–31 for 2. N-acetyl-N-demethylmayamycin (1) also inhibited the growth of methicillin-resistant Staphylococcus aureus with MIC 20.0 μM. MDPI 2016-01-06 /pmc/articles/PMC4728507/ /pubmed/26751456 http://dx.doi.org/10.3390/md14010010 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liang, Ying Xie, Xin Chen, Lu Yan, Shilun Ye, Xuewei Anjum, Komal Huang, Haocai Lian, Xiaoyuan Zhang, Zhizhen Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY |
title | Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY |
title_full | Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY |
title_fullStr | Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY |
title_full_unstemmed | Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY |
title_short | Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY |
title_sort | bioactive polycyclic quinones from marine streptomyces sp. 182smly |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728507/ https://www.ncbi.nlm.nih.gov/pubmed/26751456 http://dx.doi.org/10.3390/md14010010 |
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