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DC Field | Value | Language |
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dc.contributor.author | Yasin Mohammad, Mohammad | |
dc.contributor.author | Shakya, Ashok | |
dc.contributor.author | Al-Bakain, Ramia | |
dc.contributor.author | Haroon, M.H. | |
dc.contributor.author | Choudhary, M. Iqbal | |
dc.date.accessioned | 2018-10-10T05:25:30Z | |
dc.date.available | 2018-10-10T05:25:30Z | |
dc.date.issued | 2018-06-12 | |
dc.identifier.citation | Bioorganic Chemistry, 80: 212–215. | en_US |
dc.identifier.issn | 0045-2068 | |
dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0045206818303092 | |
dc.description.abstract | Microbial transformation of thymoquinone (5-isopropyl-2-methyl-cyclohexa-2,5-diene-1,4-dione) (1) by suspended cell-cultures of the plant pathogenic fungus Aspergillus niger resulted in the production of three metabolites. These metabolites were identified as 5-isopropyl-2-methyloxepin-1-one (2), 3-hydroxy-5-isopropyl-2- methylcyclohexa-2,5-diene-1,4-dione (3), and 5-isopropyl-2-methylbenzene-1,4-diol (4) by different spectroscopic methods. Metabolite 2 was found to be a new compound. Compound 4 showed a potent antioxidant activity. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Elsevier Publication | en_US |
dc.source.uri | https://www.sciencedirect.com/science/article/abs/pii/S0045206818303092 | |
dc.subject | Thymoquinone | en_US |
dc.subject | Aspergillus niger | en_US |
dc.subject | Fungal transformation | en_US |
dc.subject | Oxidation | en_US |
dc.subject | Reduction | en_US |
dc.subject | Antioxidant activity | en_US |
dc.title | New monoterpenoid by biotransformation of thymoquinone using Aspergillus niger | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
Files in This Item:
File | Description | Size | Format | |
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10.1016@j.bioorg.2018.06.019.pdf | 321.54 kB | Adobe PDF | View/Open |
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