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Unveiling the Mode of Action of Two Antibacterial Tanshinone Derivatives
In this study, 2-(N-pyrrolidine-alkyl) tanshinones bearing pyrrolidine groups were synthesized and the antibacterial mechanism was explored. These derivatives selectively elicited antibacterial activity against Gram-positive bacteria. Moreover, their antibacterial activities were time-, concentratio...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581214/ https://www.ncbi.nlm.nih.gov/pubmed/26263982 http://dx.doi.org/10.3390/ijms160817668 |
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author | Wang, Dongdong Zhang, Wuxia Wang, Tingting Li, Na Mu, Haibo Zhang, Jiwen Duan, Jinyou |
author_facet | Wang, Dongdong Zhang, Wuxia Wang, Tingting Li, Na Mu, Haibo Zhang, Jiwen Duan, Jinyou |
author_sort | Wang, Dongdong |
collection | PubMed |
description | In this study, 2-(N-pyrrolidine-alkyl) tanshinones bearing pyrrolidine groups were synthesized and the antibacterial mechanism was explored. These derivatives selectively elicited antibacterial activity against Gram-positive bacteria. Moreover, their antibacterial activities were time-, concentration-dependent and persistent. It appeared that Fenton-mediated hydroxyl radicals were involved, and the disruption of cell membranes was observed. This study indicates that 2-(N-pyrrolidine-alkyl) tanshinones might be potential candidates as antibacterial agents. |
format | Online Article Text |
id | pubmed-4581214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-45812142015-09-28 Unveiling the Mode of Action of Two Antibacterial Tanshinone Derivatives Wang, Dongdong Zhang, Wuxia Wang, Tingting Li, Na Mu, Haibo Zhang, Jiwen Duan, Jinyou Int J Mol Sci Article In this study, 2-(N-pyrrolidine-alkyl) tanshinones bearing pyrrolidine groups were synthesized and the antibacterial mechanism was explored. These derivatives selectively elicited antibacterial activity against Gram-positive bacteria. Moreover, their antibacterial activities were time-, concentration-dependent and persistent. It appeared that Fenton-mediated hydroxyl radicals were involved, and the disruption of cell membranes was observed. This study indicates that 2-(N-pyrrolidine-alkyl) tanshinones might be potential candidates as antibacterial agents. MDPI 2015-07-31 /pmc/articles/PMC4581214/ /pubmed/26263982 http://dx.doi.org/10.3390/ijms160817668 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Dongdong Zhang, Wuxia Wang, Tingting Li, Na Mu, Haibo Zhang, Jiwen Duan, Jinyou Unveiling the Mode of Action of Two Antibacterial Tanshinone Derivatives |
title | Unveiling the Mode of Action of Two Antibacterial Tanshinone Derivatives |
title_full | Unveiling the Mode of Action of Two Antibacterial Tanshinone Derivatives |
title_fullStr | Unveiling the Mode of Action of Two Antibacterial Tanshinone Derivatives |
title_full_unstemmed | Unveiling the Mode of Action of Two Antibacterial Tanshinone Derivatives |
title_short | Unveiling the Mode of Action of Two Antibacterial Tanshinone Derivatives |
title_sort | unveiling the mode of action of two antibacterial tanshinone derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581214/ https://www.ncbi.nlm.nih.gov/pubmed/26263982 http://dx.doi.org/10.3390/ijms160817668 |
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