Analyzing the Chemical Constituents and In Vitro Biological Effects of Extracts Artemisia absinthium L. Extracts Obtained Using Different Methodologies and Solvents
Özet
The present study aimed to investigate the chemical constituents of different extracts from aerial parts of A. absinthium and to evaluate their antioxidant and enzyme inhibition activity. Extracts were prepared by maceration, infusion or Soxhlet techniques. Results showed that the highest total phenolic and flavonoids contents was recorded respectively from the hexane extract prepared by maceration and ethyl acetate extract obtained by Soxhlet method. The characteristic compounds of Artemisia species artemetin, casticin, sesartemin and yangambin in addition to coumarins were identified in all extracts. Aqueous extract obtained by infusion exerted the highest radical scavenging and ions reducing properties while that prepared by maceration displayed the highest chelating power. Methanol extracts obtained by the two methods of extraction exerted the highest anti-Tyr activity while that obtained by maceration showed the best α-glucosidase inhibition activity. These findings indicated that A. absinthium is a rich source of bioactive molecules with possible therapeutic applications.
Anahtar Kelimeler
- Scopus
- 2
- OpenAlex
- 3
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Yagi, Sakina | |
| dc.contributor.author | Zengin, Gokhan | |
| dc.contributor.author | Ibrahime Sinan, Kouadio | |
| dc.contributor.author | Yavuz Paksoy, Mehmet | |
| dc.contributor.author | Cziáky, Zoltán | |
| dc.contributor.author | Jekő, József | |
| dc.contributor.author | Dall'Acqua, Stefano | |
| dc.date.accessioned | 2026-10-28T14:54:19.616342817Z | |
| dc.date.available | 2026-10-28T14:54:19.616342817Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | The present study aimed to investigate the chemical constituents of different extracts from aerial parts of A. absinthium and to evaluate their antioxidant and enzyme inhibition activity. Extracts were prepared by maceration, infusion or Soxhlet techniques. Results showed that the highest total phenolic and flavonoids contents was recorded respectively from the hexane extract prepared by maceration and ethyl acetate extract obtained by Soxhlet method. The characteristic compounds of Artemisia species artemetin, casticin, sesartemin and yangambin in addition to coumarins were identified in all extracts. Aqueous extract obtained by infusion exerted the highest radical scavenging and ions reducing properties while that prepared by maceration displayed the highest chelating power. Methanol extracts obtained by the two methods of extraction exerted the highest anti-Tyr activity while that obtained by maceration showed the best α-glucosidase inhibition activity. These findings indicated that A. absinthium is a rich source of bioactive molecules with possible therapeutic applications. | |
| dc.identifier.articlenumber | e202400893 | |
| dc.identifier.doi | 10.1002/cbdv.202400893 | |
| dc.identifier.eissn | 1612-1880 | |
| dc.identifier.issn | 1612-1872 | |
| dc.identifier.issue | 8 | |
| dc.identifier.pmid | 38779862 | |
| dc.identifier.scopus | 2-s2.0-85198495649 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/munzur/1547 | |
| dc.identifier.volume | 21 | |
| dc.identifier.wos | WOS:001271253600001 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Inc | |
| dc.relation.ispartof | Chemistry and Biodiversity | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | antioxidant | |
| dc.subject | Artemisia absinthium | |
| dc.subject | enzyme inhibition | |
| dc.subject | herbal medicine | |
| dc.subject | phytoconstituents | |
| dc.subject.other | alpha-Glucosidases | |
| dc.subject.other | Antioxidants | |
| dc.subject.other | Artemisia absinthium | |
| dc.subject.other | Enzyme Inhibitors | |
| dc.subject.other | Flavonoids | |
| dc.subject.other | Glycoside Hydrolase Inhibitors | |
| dc.subject.other | Phenols | |
| dc.subject.other | Plant Components, Aerial | |
| dc.subject.other | Plant Extracts | |
| dc.subject.other | Solvents | |
| dc.subject.other | 2 isopropylmalic acid | |
| dc.subject.other | 9 hydroxyoctadecadienoic acid | |
| dc.subject.other | acetic acid ethyl ester | |
| dc.subject.other | alpha glucosidase | |
| dc.subject.other | antidiabetic agent | |
| dc.subject.other | antioxidant | |
| dc.subject.other | apigenin | |
| dc.subject.other | artemetin | |
| dc.subject.other | Artemisia absinthium extract | |
| dc.subject.other | asperulosidic acid | |
| dc.subject.other | astragalin | |
| dc.subject.other | caffeic acid | |
| dc.subject.other | casticin | |
| dc.subject.other | chelating agent | |
| dc.subject.other | chlorogenic acid | |
| dc.subject.other | chryptochlorogenic acid | |
| dc.subject.other | chrysoeriol | |
| dc.subject.other | citric acid | |
| dc.subject.other | coumaric acid | |
| dc.subject.other | coumarin derivative | |
| dc.subject.other | dicaffeoylquinic acid isomer 1 | |
| dc.subject.other | dicaffeoylquinic acid isomer 2 | |
| dc.subject.other | dichloromethane | |
| dc.subject.other | dimethoxyangelicin | |
| dc.subject.other | dimethoxypsoralen | |
| dc.subject.other | dodecanedioic acid | |
| dc.subject.other | eupatilin | |
| dc.subject.other | flavonoid | |
| dc.subject.other | gentisic acid | |
| dc.subject.other | heraclenin | |
| dc.subject.other | heraclenol | |
| dc.subject.other | hexane | |
| dc.subject.other | hydroxysuberic acid | |
| dc.subject.other | isofraxidin | |
| dc.subject.other | isoimperatorin | |
| dc.subject.other | isoquercetin | |
| dc.subject.other | isorhamnetin 7 o rutinoside | |
| dc.subject.other | kaempferol | |
| dc.subject.other | kynurenic acid | |
| dc.subject.other | linolenic acid | |
| dc.subject.other | luteolin | |
| dc.subject.other | malic acid | |
| dc.subject.other | malyngic acid | |
| dc.subject.other | metal ion | |
| dc.subject.other | methanol | |
| dc.subject.other | methoxsalen | |
| dc.subject.other | neochlorogenic acid | |
| dc.subject.other | nicotiflorin | |
| dc.subject.other | pentosalen | |
| dc.subject.other | phenol derivative | |
| dc.subject.other | pheophytin A | |
| dc.subject.other | pinellic acid | |
| dc.subject.other | pranferol | |
| dc.subject.other | psoralen | |
| dc.subject.other | psoralen derivative | |
| dc.subject.other | quercetin | |
| dc.subject.other | quercetin o hexoside | |
| dc.subject.other | quinic acid | |
| dc.subject.other | rosmarinic acid | |
| dc.subject.other | rutoside | |
| dc.subject.other | saccharic acid | |
| dc.subject.other | scavenger (compound) | |
| dc.subject.other | scopoletin | |
| dc.subject.other | sesartemin | |
| dc.subject.other | solvent | |
| dc.subject.other | spinacetin 3 o glucoside | |
| dc.subject.other | spinacetin 3 o rutinoside | |
| dc.subject.other | spinacetin o hexoside | |
| dc.subject.other | syringic acid | |
| dc.subject.other | tetrahydroxy flavone o rhamnosylhexoside | |
| dc.subject.other | traumatic acid | |
| dc.subject.other | trihydroxy trimethoxy flavone isomer 2 | |
| dc.subject.other | trihydroxy trimethoxy iso flavone isomer 1 | |
| dc.subject.other | tuberonic acid | |
| dc.subject.other | tuberonic acid sulfate | |
| dc.subject.other | unclassified drug | |
| dc.subject.other | undecanedioic acid | |
| dc.subject.other | vanillic acid | |
| dc.subject.other | yangambin | |
| dc.subject.other | enzyme inhibitor | |
| dc.subject.other | glycosidase inhibitor | |
| dc.subject.other | plant extract | |
| dc.subject.other | Alzheimer disease | |
| dc.subject.other | analytic method | |
| dc.subject.other | antidiabetic activity | |
| dc.subject.other | antioxidant activity | |
| dc.subject.other | Article | |
| dc.subject.other | chemical composition | |
| dc.subject.other | controlled study | |
| dc.subject.other | diabetes mellitus | |
| dc.title | Analyzing the Chemical Constituents and In Vitro Biological Effects of Extracts Artemisia absinthium L. Extracts Obtained Using Different Methodologies and Solvents | |
| dc.type | Article | |
| rdl.citation.openalex | 3 | |
| rdl.citation.scopus | 2 | |
| rdl.department | Department of Botany, Faculty of Science, University of Khartoum, Khartoum, Sudan | |
| rdl.department | Université de Lorraine, INRAE, LAE, F-54000, Nancy, France | |
| rdl.department | Department of Biology, Faculty of Science, Selcuk University, Konya, Turkey | |
| rdl.department | Munzur University, Tunceli Vocational School, Medical Documentation and Secretaryship Pr., Tunceli, Turkey | |
| rdl.department | Agricultural and Molecular Research and Service Institute, University of Nyíregyháza, Nyíregyháza, Hungary | |
| rdl.department | Department of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131, Padua, Italy | |
| rdl.oa.status | closed | |
| rdl.scopus.quartile | Q3 | |
| rdl.sdg | SDG03 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED |

