Flavonoids from Chromolaena odorata (Linn.) King & H. Rob
Chromolaena odorata (Linn.) King & H. Rob. afforded 5,6,7,4- tetramethoxyflavone (C-14) and 4-hydroxy-5,6,7-trimethoxyflavanone (C-16). The structures of the two flavonoids were elucidated by extensive 1D and 2D NMR spectroscopy. The structure of C-16 was confirmed by comparison of its 1H NMR sp...
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oai:animorepository.dlsu.edu.ph:etd_masteral-103212023-09-21T09:21:43Z Flavonoids from Chromolaena odorata (Linn.) King & H. Rob Cuarto, Ceazar Ryan Umali Chromolaena odorata (Linn.) King & H. Rob. afforded 5,6,7,4- tetramethoxyflavone (C-14) and 4-hydroxy-5,6,7-trimethoxyflavanone (C-16). The structures of the two flavonoids were elucidated by extensive 1D and 2D NMR spectroscopy. The structure of C-16 was confirmed by comparison of its 1H NMR spectral data with those reported in the literature. C-14 was tested for antimicrobial potential by the agar well method against seven microorganisms. Results of the study indicated low antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and low antifungal activity against Candida albicans and Trichophyton mentagrophytes. It was found inactive against Bacillus subtilis and Aspergillus niger. 2007-01-01T08:00:00Z text application/pdf https://animorepository.dlsu.edu.ph/etd_masteral/3483 https://animorepository.dlsu.edu.ph/context/etd_masteral/article/10321/viewcontent/CDTG004227_P.pdf Master's Theses English Animo Repository Flavonoids Chromolaena odorata Dichloromethane |
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Flavonoids Chromolaena odorata Dichloromethane Cuarto, Ceazar Ryan Umali Flavonoids from Chromolaena odorata (Linn.) King & H. Rob |
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Chromolaena odorata (Linn.) King & H. Rob. afforded 5,6,7,4- tetramethoxyflavone (C-14) and 4-hydroxy-5,6,7-trimethoxyflavanone (C-16). The structures of the two flavonoids were elucidated by extensive 1D and 2D NMR spectroscopy. The structure of C-16 was confirmed by comparison of its 1H NMR spectral data with those reported in the literature.
C-14 was tested for antimicrobial potential by the agar well method against seven microorganisms. Results of the study indicated low antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and low antifungal activity against Candida albicans and Trichophyton mentagrophytes. It was found inactive against Bacillus subtilis and Aspergillus niger. |
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Cuarto, Ceazar Ryan Umali |
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Cuarto, Ceazar Ryan Umali |
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Cuarto, Ceazar Ryan Umali |
title |
Flavonoids from Chromolaena odorata (Linn.) King & H. Rob |
title_short |
Flavonoids from Chromolaena odorata (Linn.) King & H. Rob |
title_full |
Flavonoids from Chromolaena odorata (Linn.) King & H. Rob |
title_fullStr |
Flavonoids from Chromolaena odorata (Linn.) King & H. Rob |
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Flavonoids from Chromolaena odorata (Linn.) King & H. Rob |
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flavonoids from chromolaena odorata (linn.) king & h. rob |
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Animo Repository |
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2007 |
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https://animorepository.dlsu.edu.ph/etd_masteral/3483 https://animorepository.dlsu.edu.ph/context/etd_masteral/article/10321/viewcontent/CDTG004227_P.pdf |
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