Concise synthesis of quercetagetin (3,3ʹ,4ʹ,5,6,7-hexahydroxyflavone) with antioxidant and antibacterial activities
[Display omitted] •A concise, efficient, and scalable synthesis of quercetagetin was reported.•The antioxidant activity was investigated using radical scavenging assays.•Synthetic quercetagetin displayed potent antibacterial activity against MRSA strains. Quercetagetin (3,3ʹ,4ʹ,5,6,7-hexahydroxyflav...
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Published in | Results in Chemistry Vol. 3; p. 100255 |
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Abstract | [Display omitted]
•A concise, efficient, and scalable synthesis of quercetagetin was reported.•The antioxidant activity was investigated using radical scavenging assays.•Synthetic quercetagetin displayed potent antibacterial activity against MRSA strains.
Quercetagetin (3,3ʹ,4ʹ,5,6,7-hexahydroxyflavone) is a characteristic flavonol that has six hydroxy (–OH) group based on the chemical structure of the flavone backbone. Herein, we report a concise, efficient, and scalable synthesis of biologically important quercetagetin with antioxidant and antibacterial activities. The synthesis has been achieved in three steps from starting materials 1 and 2 in 27 % overall yield. The chemical structure of synthetic quercetagetin has been confirmed by 1H NMR, 13C NMR, and high-resolution mass spectrometry (HRMS) analyses. Antioxidant activity of synthetic quercetagetin and control compounds quercetin, butylated hydroxyanisole (BHA), and Trolox has been compared using DPPH and ABTS radical scavenging assays. The synthetic quercetagetin exhibits the highest antioxidant activity when compared with control compounds. Furthermore, the synthetic quercetagetin has displayed potent antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) strains with MIC value of 16 µg/mL when compared with standard antibiotic drugs Ampicillin and Kanamycin (with MIC values of >256 µg/mL). To distinguish bactericidal and bacteriostatic effects of synthetic quercetagetin, time-kill kinetic studies have been performed and the results exhibit that the synthetic quercetagetin possesses bacteriostatic action. |
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AbstractList | [Display omitted]
•A concise, efficient, and scalable synthesis of quercetagetin was reported.•The antioxidant activity was investigated using radical scavenging assays.•Synthetic quercetagetin displayed potent antibacterial activity against MRSA strains.
Quercetagetin (3,3ʹ,4ʹ,5,6,7-hexahydroxyflavone) is a characteristic flavonol that has six hydroxy (–OH) group based on the chemical structure of the flavone backbone. Herein, we report a concise, efficient, and scalable synthesis of biologically important quercetagetin with antioxidant and antibacterial activities. The synthesis has been achieved in three steps from starting materials 1 and 2 in 27 % overall yield. The chemical structure of synthetic quercetagetin has been confirmed by 1H NMR, 13C NMR, and high-resolution mass spectrometry (HRMS) analyses. Antioxidant activity of synthetic quercetagetin and control compounds quercetin, butylated hydroxyanisole (BHA), and Trolox has been compared using DPPH and ABTS radical scavenging assays. The synthetic quercetagetin exhibits the highest antioxidant activity when compared with control compounds. Furthermore, the synthetic quercetagetin has displayed potent antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) strains with MIC value of 16 µg/mL when compared with standard antibiotic drugs Ampicillin and Kanamycin (with MIC values of >256 µg/mL). To distinguish bactericidal and bacteriostatic effects of synthetic quercetagetin, time-kill kinetic studies have been performed and the results exhibit that the synthetic quercetagetin possesses bacteriostatic action. Quercetagetin (3,3ʹ,4ʹ,5,6,7-hexahydroxyflavone) is a characteristic flavonol that has six hydroxy (–OH) group based on the chemical structure of the flavone backbone. Herein, we report a concise, efficient, and scalable synthesis of biologically important quercetagetin with antioxidant and antibacterial activities. The synthesis has been achieved in three steps from starting materials 1 and 2 in 27 % overall yield. The chemical structure of synthetic quercetagetin has been confirmed by 1H NMR, 13C NMR, and high-resolution mass spectrometry (HRMS) analyses. Antioxidant activity of synthetic quercetagetin and control compounds quercetin, butylated hydroxyanisole (BHA), and Trolox has been compared using DPPH and ABTS radical scavenging assays. The synthetic quercetagetin exhibits the highest antioxidant activity when compared with control compounds. Furthermore, the synthetic quercetagetin has displayed potent antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) strains with MIC value of 16 µg/mL when compared with standard antibiotic drugs Ampicillin and Kanamycin (with MIC values of >256 µg/mL). To distinguish bactericidal and bacteriostatic effects of synthetic quercetagetin, time-kill kinetic studies have been performed and the results exhibit that the synthetic quercetagetin possesses bacteriostatic action. |
ArticleNumber | 100255 |
Author | Deniz Yilmaz, M. Bulut, Onur |
Author_xml | – sequence: 1 givenname: Onur surname: Bulut fullname: Bulut, Onur email: onur.bulut@gidatarim.edu.tr organization: Department of Bioengineering, Faculty of Engineering and Architecture, Konya Food and Agriculture University, 42080 Konya, Turkey – sequence: 2 givenname: M. surname: Deniz Yilmaz fullname: Deniz Yilmaz, M. email: deniz.yilmaz@gidatarim.edu.tr organization: Department of Bioengineering, Faculty of Engineering and Architecture, Konya Food and Agriculture University, 42080 Konya, Turkey |
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CitedBy_id | crossref_primary_10_3389_fchem_2024_1411801 crossref_primary_10_3390_molecules29020513 crossref_primary_10_1021_acsabm_3c00021 crossref_primary_10_3390_ph16111543 crossref_primary_10_1021_acsanm_2c00834 crossref_primary_10_1016_j_ijpharm_2022_122093 |
Cites_doi | 10.1021/jf0620719 10.1007/s13205-013-0117-5 10.1016/S0031-9422(00)84689-0 10.1158/1535-7163.MCT-06-0397 10.4172/pharmaceutical-sciences.1000299 10.1021/np9904509 10.2174/187152810793358741 10.1007/s11164-016-2797-z 10.1002/ptr.6208 10.3390/ijms12128895 10.1016/j.foodchem.2014.05.125 10.1016/j.intimp.2007.05.004 10.1007/BF03172537 10.4067/S0716-97602000000200007 10.1007/s13197-016-2228-6 10.1002/jmv.1890150110 10.1016/j.plaphy.2007.12.009 10.1093/nar/gku632 10.1021/jf053071w 10.1007/s11094-019-01939-8 10.1002/jcp.25026 10.3987/R-1986-04-1099 10.1016/j.fitote.2011.12.013 10.1021/cr00032a005 10.4062/biomolther.2013.001 10.1016/j.ijantimicag.2005.09.002 10.1016/j.tet.2017.06.064 |
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Keywords | Flavonols Flavonoids Antibacterial Antioxidant Quercetagetin |
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•A concise, efficient, and scalable synthesis of quercetagetin was reported.•The antioxidant activity was investigated using radical... Quercetagetin (3,3ʹ,4ʹ,5,6,7-hexahydroxyflavone) is a characteristic flavonol that has six hydroxy (–OH) group based on the chemical structure of the flavone... |
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SubjectTerms | Antibacterial Antioxidant Flavonoids Flavonols Quercetagetin |
Title | Concise synthesis of quercetagetin (3,3ʹ,4ʹ,5,6,7-hexahydroxyflavone) with antioxidant and antibacterial activities |
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