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New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells
Seven new azalomycin F analogs (1–7) were isolated from the broth of mangrove Streptomyces sp. 211726, and respectively identified as 25-malonyl demalonylazalomycin F(5a) monoester (1), 23-valine demalonylazalomycin F(5a) ester (2), 23-(6-methyl)heptanoic acid demalonylazalomycins F(3a) ester (3), F...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3705372/ https://www.ncbi.nlm.nih.gov/pubmed/23481678 http://dx.doi.org/10.3390/md11030817 |
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author | Yuan, Ganjun Hong, Kui Lin, Haipeng She, Zhigang Li, Jia |
author_facet | Yuan, Ganjun Hong, Kui Lin, Haipeng She, Zhigang Li, Jia |
author_sort | Yuan, Ganjun |
collection | PubMed |
description | Seven new azalomycin F analogs (1–7) were isolated from the broth of mangrove Streptomyces sp. 211726, and respectively identified as 25-malonyl demalonylazalomycin F(5a) monoester (1), 23-valine demalonylazalomycin F(5a) ester (2), 23-(6-methyl)heptanoic acid demalonylazalomycins F(3a) ester (3), F(4a) ester (4) and F(5a) ester (5), 23-(9-methyl)decanoic acid demalonylazalomycin F(4a) ester (6) and 23-(10-methyl)undecanoic acid demalonylazalomycin F(4a) ester (7). Their structures were established by their spectroscopic data and by comparing with those of azalomycins F(3a), F(4a) and F(5a). Biological assays exhibited that 1–7 showed broad-spectrum antimicrobial and anti HCT-116 activities. |
format | Online Article Text |
id | pubmed-3705372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-37053722013-07-09 New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells Yuan, Ganjun Hong, Kui Lin, Haipeng She, Zhigang Li, Jia Mar Drugs Article Seven new azalomycin F analogs (1–7) were isolated from the broth of mangrove Streptomyces sp. 211726, and respectively identified as 25-malonyl demalonylazalomycin F(5a) monoester (1), 23-valine demalonylazalomycin F(5a) ester (2), 23-(6-methyl)heptanoic acid demalonylazalomycins F(3a) ester (3), F(4a) ester (4) and F(5a) ester (5), 23-(9-methyl)decanoic acid demalonylazalomycin F(4a) ester (6) and 23-(10-methyl)undecanoic acid demalonylazalomycin F(4a) ester (7). Their structures were established by their spectroscopic data and by comparing with those of azalomycins F(3a), F(4a) and F(5a). Biological assays exhibited that 1–7 showed broad-spectrum antimicrobial and anti HCT-116 activities. MDPI 2013-03-12 /pmc/articles/PMC3705372/ /pubmed/23481678 http://dx.doi.org/10.3390/md11030817 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Yuan, Ganjun Hong, Kui Lin, Haipeng She, Zhigang Li, Jia New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells |
title | New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells |
title_full | New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells |
title_fullStr | New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells |
title_full_unstemmed | New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells |
title_short | New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells |
title_sort | new azalomycin f analogs from mangrove streptomyces sp. 211726 with activity against microbes and cancer cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3705372/ https://www.ncbi.nlm.nih.gov/pubmed/23481678 http://dx.doi.org/10.3390/md11030817 |
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