Isolation, identification of secondary metabolites from Salvia absconditiflora and evaluation of their antioxidative properties
Özet
Salvia absconditiflora Greuter & Burdet (Synonym Salvia cryptantha Montbret & Aucher ex Benth) has been used extensively for traditional medicine. The aerial of plant material was boiled in water then filtrated. The filtrate was partitioned with ethyl acetate and n-butanol sequentially to yield the ethyl acetate and n-butanol extract. A sample of water was lyophilized to yield the water extract. Ethyl acetate extract revealed the highest antioxidant activity and included the most phenolic compounds among the extracts. Hence, ethyl acetate extract was subjected to chromatographic techniques. Ursolic acid (1), crismaritin (2), luteolin (3), rosmarinic acid methyl ester (4), 3,4-dihydroxyl benzaldehyde (protocatechuic aldehyde) (5), caffeic acid (6), apigenin-7-O-β-glucoside (7), rosmarinic acid (8) and luteolin-7-O-β-glucoside (9) were isolated and the structures were elucidated by spectroscopic methods including 1D, 2D NMR, and LC-TOF/MS. Cirsimaritin (2), luteolin (3), rosmarinic acid methyl ester (4), rosmarinic acid (8), luteolin-7-O-β-glucoside (9) displayed the considerable antioxidant activity. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Koysu, Perihan | |
| dc.contributor.author | Genc, Nusret | |
| dc.contributor.author | Elmastas, Mahfuz | |
| dc.contributor.author | Aksit, Huseyin | |
| dc.contributor.author | Erenler, Ramazan | |
| dc.date.accessioned | 2026-10-18T20:28:45.134868680Z | |
| dc.date.available | 2026-10-18T20:28:45.134868680Z | |
| dc.date.issued | 2019 | |
| dc.description.abstract | Salvia absconditiflora Greuter & Burdet (Synonym Salvia cryptantha Montbret & Aucher ex Benth) has been used extensively for traditional medicine. The aerial of plant material was boiled in water then filtrated. The filtrate was partitioned with ethyl acetate and n-butanol sequentially to yield the ethyl acetate and n-butanol extract. A sample of water was lyophilized to yield the water extract. Ethyl acetate extract revealed the highest antioxidant activity and included the most phenolic compounds among the extracts. Hence, ethyl acetate extract was subjected to chromatographic techniques. Ursolic acid (1), crismaritin (2), luteolin (3), rosmarinic acid methyl ester (4), 3,4-dihydroxyl benzaldehyde (protocatechuic aldehyde) (5), caffeic acid (6), apigenin-7-O-β-glucoside (7), rosmarinic acid (8) and luteolin-7-O-β-glucoside (9) were isolated and the structures were elucidated by spectroscopic methods including 1D, 2D NMR, and LC-TOF/MS. Cirsimaritin (2), luteolin (3), rosmarinic acid methyl ester (4), rosmarinic acid (8), luteolin-7-O-β-glucoside (9) displayed the considerable antioxidant activity. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group. | |
| dc.description.sponsorship | This work was supported by Gaziosmanpasa University Research Fund (No: 2015-87). | |
| dc.identifier.doi | 10.1080/14786419.2018.1488700 | |
| dc.identifier.eissn | 1478-6427 | |
| dc.identifier.endpage | 3595 | |
| dc.identifier.issn | 1478-6419 | |
| dc.identifier.issue | 24 | |
| dc.identifier.pmid | 30445824 | |
| dc.identifier.scopus | 2-s2.0-85057224204 | |
| dc.identifier.startpage | 3592 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/13952 | |
| dc.identifier.volume | 33 | |
| dc.identifier.wos | WOS:000491239200021 | |
| dc.language.iso | en | |
| dc.publisher | Taylor and Francis Ltd. | |
| dc.relation.ispartof | Natural Product Research | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | chromatography | |
| dc.subject | natural products | |
| dc.subject | Salvia absconditiflora | |
| dc.subject | spectroscopy | |
| dc.subject | Antioxidants | |
| dc.subject | Apigenin | |
| dc.subject | Caffeic Acids | |
| dc.subject | Cinnamates | |
| dc.subject | Depsides | |
| dc.subject | Flavones | |
| dc.subject | Glucosides | |
| dc.subject | Luteolin | |
| dc.subject | Molecular Structure | |
| dc.subject | Phenols | |
| dc.subject | Plant Extracts | |
| dc.subject | Salvia | |
| dc.subject | Spectrum Analysis | |
| dc.subject | 3,4 dihydroxyl benzaldehyde | |
| dc.subject | acetic acid ethyl ester | |
| dc.subject | antioxidant | |
| dc.subject | apigenin 7 o beta glucoside | |
| dc.subject | butanol | |
| dc.subject | caffeic acid | |
| dc.subject | crismaritin | |
| dc.subject | drug metabolite | |
| dc.subject | luteolin 7 o beta glucoside | |
| dc.subject | phenol derivative | |
| dc.subject | plant extract | |
| dc.subject | rosmarinic acid | |
| dc.subject | rosmarinic acid methyl ester | |
| dc.title | Isolation, identification of secondary metabolites from Salvia absconditiflora and evaluation of their antioxidative properties | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 28 | |
| rdl.citation.wos | 24 | |
| rdl.department | Department of Analytical Chemistry, Faculty of Pharmacy, Erzincan University , Erzincan , Turkey. | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
