Undescribed and known phenolic acid derivatives with significant antioxidant activity from the Scorzonera parviflora Jacq. roots
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
39645051
DOI
10.1016/j.fitote.2024.106328
PII: S0367-326X(24)00511-2
Knihovny.cz E-resources
- Keywords
- Antioxidant activity, Asteraceae, Phenolic acids, Scorzonera parviflora, Sesquiterpene lactone,
- MeSH
- Antioxidants * pharmacology isolation & purification chemistry MeSH
- Phytochemicals pharmacology isolation & purification MeSH
- Hydroxybenzoates * isolation & purification pharmacology chemistry MeSH
- Plant Roots * chemistry MeSH
- Molecular Structure MeSH
- Scorzonera * chemistry MeSH
- Sesquiterpenes pharmacology isolation & purification chemistry MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antioxidants * MeSH
- Phytochemicals MeSH
- Hydroxybenzoates * MeSH
- phenolic acid MeSH Browser
- Sesquiterpenes MeSH
The antioxidant activity of Scorzonera parviflora Jacq. roots were assessed by measuring their ability to scavenge ABTS and DPPH radicals. Bioactivity-guided fractionation was utilized to identify the compound(s) responsible for this activity. The most active phase, ethyl acetate, was isolated using column chromatography. The resulting fractions were then purified using preparative TLC on reverse phase and semi-preparative HPLC. The structures of the pure compounds were elucidated by spectral analysis (MS and 1H, 13C, 2D-NMR). Three undescribed phenolic acid derivatives, namely parvifloric acid A (1), B (2), and C (3), and one new sesquiterpene lactone, parviflorin (4) together with seven known compounds were isolated and identified as scopolin (5), scopoletin (6), caffeic acid (7), protocatechuic acid (8), 4,5-O-dicaffeoylquinic acid (9) 3,5-O-dicaffeoylquinic acid (10), and 3,5-O-dicaffeoylquinic acid methyl ester (11). Finally, the pure compounds obtained were tested to evaluate their antioxidant capacities, using ABTS and DPPH radical scavenging potencies. The highest activity was observed with 3,5-O-dicaffeoylquinic acid (10), followed by its methyl ester.
Ankara University Faculty of Pharmacy Department of Pharmacognosy Tandogan 06100 Ankara Turkey
Bulent Ecevit University Faculty of Pharmacy Department of Pharmacognosy Zonguldak Turkey
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