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Antibacterial activity of thymoquinone derivative
Natural products such as terpenoidal compounds have been extremely tested against pathogenic bacteria. Researches are frequently carried out to find out new natural, semisynthetic and synthetic antibacterial agents due to problems of resistance. Thymoquinone derivative was obtained in our previous s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557212/ https://www.ncbi.nlm.nih.gov/pubmed/37798782 http://dx.doi.org/10.1186/s13104-023-06523-8 |
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author | Mohammad, Mohammad Yasin Haniffa, Haroon M. Choudhary, M. Iqbal |
author_facet | Mohammad, Mohammad Yasin Haniffa, Haroon M. Choudhary, M. Iqbal |
author_sort | Mohammad, Mohammad Yasin |
collection | PubMed |
description | Natural products such as terpenoidal compounds have been extremely tested against pathogenic bacteria. Researches are frequently carried out to find out new natural, semisynthetic and synthetic antibacterial agents due to problems of resistance. Thymoquinone derivative was obtained in our previous study and the current research is a continuation. The antibacterial activity of a monoterpenoid; thymoquinone derivative, 5-isopropyl-2-methyloxepine-1-one (1) has been evaluated for the first time by following the Agar cup bioassay method employed. The bacterial strains used in this study were Escherichia coli and Bacillus subtilis. Compound 1 showed moderate activity against Gram-positive organism; B. subtilis and good activity against Gram-negative species; E. coli with zones of inhibition (ZOI) 10.0 ± 0.2 mm and 11.0 ± 0.2 mm against E. coli and B. subtilis, respectively, and in comparison with antibiotic, imipenem. The zones of inhibition were calculated as the mean of the triplicate. The antibacterial activity of thymoquinone derivative 1 could be explained by the presence of unsaturated lactone. |
format | Online Article Text |
id | pubmed-10557212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105572122023-10-07 Antibacterial activity of thymoquinone derivative Mohammad, Mohammad Yasin Haniffa, Haroon M. Choudhary, M. Iqbal BMC Res Notes Research Note Natural products such as terpenoidal compounds have been extremely tested against pathogenic bacteria. Researches are frequently carried out to find out new natural, semisynthetic and synthetic antibacterial agents due to problems of resistance. Thymoquinone derivative was obtained in our previous study and the current research is a continuation. The antibacterial activity of a monoterpenoid; thymoquinone derivative, 5-isopropyl-2-methyloxepine-1-one (1) has been evaluated for the first time by following the Agar cup bioassay method employed. The bacterial strains used in this study were Escherichia coli and Bacillus subtilis. Compound 1 showed moderate activity against Gram-positive organism; B. subtilis and good activity against Gram-negative species; E. coli with zones of inhibition (ZOI) 10.0 ± 0.2 mm and 11.0 ± 0.2 mm against E. coli and B. subtilis, respectively, and in comparison with antibiotic, imipenem. The zones of inhibition were calculated as the mean of the triplicate. The antibacterial activity of thymoquinone derivative 1 could be explained by the presence of unsaturated lactone. BioMed Central 2023-10-06 /pmc/articles/PMC10557212/ /pubmed/37798782 http://dx.doi.org/10.1186/s13104-023-06523-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Note Mohammad, Mohammad Yasin Haniffa, Haroon M. Choudhary, M. Iqbal Antibacterial activity of thymoquinone derivative |
title | Antibacterial activity of thymoquinone derivative |
title_full | Antibacterial activity of thymoquinone derivative |
title_fullStr | Antibacterial activity of thymoquinone derivative |
title_full_unstemmed | Antibacterial activity of thymoquinone derivative |
title_short | Antibacterial activity of thymoquinone derivative |
title_sort | antibacterial activity of thymoquinone derivative |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557212/ https://www.ncbi.nlm.nih.gov/pubmed/37798782 http://dx.doi.org/10.1186/s13104-023-06523-8 |
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