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Salumycin, a New Pyrazolequinone from a Streptomyces albus J1074 Mutant Strain
Heterocyclic natural products with various bioactivities play significant roles in pharmaceuticals. Here, we isolated a heterocyclic compound salumycin (1) from a Streptomyces albus J1074 mutant strain. The structure of (1) was elucidated via single-crystal X-ray diffraction, mass spectrometry (MS),...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7570766/ https://www.ncbi.nlm.nih.gov/pubmed/32911655 http://dx.doi.org/10.3390/molecules25184098 |
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author | Tao, Kaixiang Ye, Taijia Cao, Mingming Meng, Xiaolu Li, Yuqing Wang, Huan Feng, Zhiyang |
author_facet | Tao, Kaixiang Ye, Taijia Cao, Mingming Meng, Xiaolu Li, Yuqing Wang, Huan Feng, Zhiyang |
author_sort | Tao, Kaixiang |
collection | PubMed |
description | Heterocyclic natural products with various bioactivities play significant roles in pharmaceuticals. Here, we isolated a heterocyclic compound salumycin (1) from a Streptomyces albus J1074 mutant strain. The structure of (1) was elucidated via single-crystal X-ray diffraction, mass spectrometry (MS), fourier transform infrared spectrometer (FTIR), and nuclear magnetic resonance (NMR) data analysis. Salumycin (1) contained a novel pyrazolequinone ring, which had never been previously reported in a natural product. Salumycin (1) exhibited moderate 2,2′-diphenyl-1-picrylhydrazyl (DPPH)-radical scavenging activity (EC50 = 46.3 ± 2.2 μM) compared with tert-butylhydroquinone (EC50 = 4.7 ± 0.3 μM). This study provides a new example of discovering novel natural products from bacteria. |
format | Online Article Text |
id | pubmed-7570766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75707662020-10-28 Salumycin, a New Pyrazolequinone from a Streptomyces albus J1074 Mutant Strain Tao, Kaixiang Ye, Taijia Cao, Mingming Meng, Xiaolu Li, Yuqing Wang, Huan Feng, Zhiyang Molecules Communication Heterocyclic natural products with various bioactivities play significant roles in pharmaceuticals. Here, we isolated a heterocyclic compound salumycin (1) from a Streptomyces albus J1074 mutant strain. The structure of (1) was elucidated via single-crystal X-ray diffraction, mass spectrometry (MS), fourier transform infrared spectrometer (FTIR), and nuclear magnetic resonance (NMR) data analysis. Salumycin (1) contained a novel pyrazolequinone ring, which had never been previously reported in a natural product. Salumycin (1) exhibited moderate 2,2′-diphenyl-1-picrylhydrazyl (DPPH)-radical scavenging activity (EC50 = 46.3 ± 2.2 μM) compared with tert-butylhydroquinone (EC50 = 4.7 ± 0.3 μM). This study provides a new example of discovering novel natural products from bacteria. MDPI 2020-09-08 /pmc/articles/PMC7570766/ /pubmed/32911655 http://dx.doi.org/10.3390/molecules25184098 Text en © 2020 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 | Communication Tao, Kaixiang Ye, Taijia Cao, Mingming Meng, Xiaolu Li, Yuqing Wang, Huan Feng, Zhiyang Salumycin, a New Pyrazolequinone from a Streptomyces albus J1074 Mutant Strain |
title | Salumycin, a New Pyrazolequinone from a Streptomyces albus J1074 Mutant Strain |
title_full | Salumycin, a New Pyrazolequinone from a Streptomyces albus J1074 Mutant Strain |
title_fullStr | Salumycin, a New Pyrazolequinone from a Streptomyces albus J1074 Mutant Strain |
title_full_unstemmed | Salumycin, a New Pyrazolequinone from a Streptomyces albus J1074 Mutant Strain |
title_short | Salumycin, a New Pyrazolequinone from a Streptomyces albus J1074 Mutant Strain |
title_sort | salumycin, a new pyrazolequinone from a streptomyces albus j1074 mutant strain |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7570766/ https://www.ncbi.nlm.nih.gov/pubmed/32911655 http://dx.doi.org/10.3390/molecules25184098 |
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