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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...

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Detalles Bibliográficos
Autores principales: Liang, Ying, Xie, Xin, Chen, Lu, Yan, Shilun, Ye, Xuewei, Anjum, Komal, Huang, Haocai, Lian, Xiaoyuan, Zhang, Zhizhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
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
Descripción
Sumario: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.