Combining chemical profiles and biological abilities of different extracts from Tanacetum nitens (Boiss. & Noë) Grierson using network pharmacology
Özet
Tanacetum nitens (Boiss. & Noë) Grierson is an aromatic perennial herb used in Turkish traditional medicine to treat headache, fever, and skin diseases. This study aimed to investigate the chemical composition, antioxidant, enzyme inhibition, and cytotoxic properties of T. nitens aerial parts. Organic solvent extracts were prepared by sequential maceration in hexane, dichloromethane, ethyl acetate, and methanol while aqueous extracts were obtained by maceration or infusion. Nuclear magnetic resonance (NMR) and LC-DAD-MS analysis allowed the identification and quantification of different phytoconstituents including parthenolide, tanacetol B, tatridin B, quinic acid derivatives, β-sitosterol, and glycoside derivatives of quercetin and luteolin. The type and amount of these phytochemicals recovered by each solvent were variable and significant enough to impact the biological activities of the plant. Methanolic and aqueous extracts displayed the highest scavenging and ions-reducing properties while the dichloromethane and ethyl acetate extracts exerted the best total antioxidant activity and metal chelating power. Results of enzyme inhibition activity showed that the hexane, ethyl acetate, and dichloromethane extracts had comparable anti-acetylcholinesterase activity and the latter extract revealed the highest anti-butyrylcholinesterase activity. The best α-amylase and α-glucosidase inhibition activities were obtained from the hexane extract. The dichloromethane and ethyl acetate extracts exhibited the highest cytotoxic effect against the prostate carcinoma DU-145 cells. In conclusion, these findings indicated that T. nitens can be a promising source of biomolecules with potential therapeutic applications.
Anahtar Kelimeler
- Scopus
- 7
- OpenAlex
- 7
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Dall'Acqua, Stefano | |
| dc.contributor.author | Yagi, Sakina | |
| dc.contributor.author | Sut, Stefania | |
| dc.contributor.author | Uba, Abdullahi Ibrahim | |
| dc.contributor.author | Ponniya, Sathish Kumar M. | |
| dc.contributor.author | Koyuncu, Ismail | |
| dc.contributor.author | Toprak, Kenan | |
| dc.contributor.author | Balos, Mehmet Maruf | |
| dc.contributor.author | Kaplan, Alevcan | |
| dc.contributor.author | Çakılcıoğlu, Uğur | |
| dc.contributor.author | Zengin, Gokhan | |
| dc.date.accessioned | 2026-10-28T14:54:53.871122145Z | |
| dc.date.available | 2026-10-28T14:54:53.871122145Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | Tanacetum nitens (Boiss. & Noë) Grierson is an aromatic perennial herb used in Turkish traditional medicine to treat headache, fever, and skin diseases. This study aimed to investigate the chemical composition, antioxidant, enzyme inhibition, and cytotoxic properties of T. nitens aerial parts. Organic solvent extracts were prepared by sequential maceration in hexane, dichloromethane, ethyl acetate, and methanol while aqueous extracts were obtained by maceration or infusion. Nuclear magnetic resonance (NMR) and LC-DAD-MS analysis allowed the identification and quantification of different phytoconstituents including parthenolide, tanacetol B, tatridin B, quinic acid derivatives, β-sitosterol, and glycoside derivatives of quercetin and luteolin. The type and amount of these phytochemicals recovered by each solvent were variable and significant enough to impact the biological activities of the plant. Methanolic and aqueous extracts displayed the highest scavenging and ions-reducing properties while the dichloromethane and ethyl acetate extracts exerted the best total antioxidant activity and metal chelating power. Results of enzyme inhibition activity showed that the hexane, ethyl acetate, and dichloromethane extracts had comparable anti-acetylcholinesterase activity and the latter extract revealed the highest anti-butyrylcholinesterase activity. The best α-amylase and α-glucosidase inhibition activities were obtained from the hexane extract. The dichloromethane and ethyl acetate extracts exhibited the highest cytotoxic effect against the prostate carcinoma DU-145 cells. In conclusion, these findings indicated that T. nitens can be a promising source of biomolecules with potential therapeutic applications. | |
| dc.identifier.articlenumber | 2400194 | |
| dc.identifier.doi | 10.1002/ardp.202400194 | |
| dc.identifier.eissn | 1521-4184 | |
| dc.identifier.issn | 0365-6233 | |
| dc.identifier.issue | 9 | |
| dc.identifier.pmid | 38877616 | |
| dc.identifier.scopus | 2-s2.0-85196076146 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/munzur/2066 | |
| dc.identifier.volume | 357 | |
| dc.identifier.wos | WOS:001250133500001 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Inc | |
| dc.relation.ispartof | Archiv der Pharmazie | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | antioxidant | |
| dc.subject | cytotoxicity | |
| dc.subject | enzyme inhibition | |
| dc.subject | phytoconstituents | |
| dc.subject | Tanacetum nitens | |
| dc.subject.other | Antineoplastic Agents, Phytogenic | |
| dc.subject.other | Antioxidants | |
| dc.subject.other | Cell Line, Tumor | |
| dc.subject.other | Cell Survival | |
| dc.subject.other | Dose-Response Relationship, Drug | |
| dc.subject.other | Humans | |
| dc.subject.other | Phytochemicals | |
| dc.subject.other | Plant Components, Aerial | |
| dc.subject.other | Plant Extracts | |
| dc.subject.other | Solvents | |
| dc.subject.other | Tanacetum | |
| dc.subject.other | acetic acid ethyl ester | |
| dc.subject.other | acetylcholinesterase | |
| dc.subject.other | alglucosidase alfa | |
| dc.subject.other | alpha glucosidase | |
| dc.subject.other | amylase | |
| dc.subject.other | cholinesterase | |
| dc.subject.other | dichloromethane | |
| dc.subject.other | glucosidase | |
| dc.subject.other | glycoside | |
| dc.subject.other | hexane | |
| dc.subject.other | luteolin | |
| dc.subject.other | methanol | |
| dc.subject.other | monophenol monooxygenase | |
| dc.subject.other | organic solvent | |
| dc.subject.other | parthenolide | |
| dc.subject.other | phytochemical | |
| dc.subject.other | plant extract | |
| dc.subject.other | quercetin | |
| dc.subject.other | quinic acid | |
| dc.subject.other | sitosterol | |
| dc.subject.other | tanacetol B | |
| dc.subject.other | Tanacetum nitens extract | |
| dc.subject.other | tatridin B | |
| dc.subject.other | unclassified drug | |
| dc.subject.other | antineoplastic agent | |
| dc.subject.other | antioxidant | |
| dc.subject.other | solvent | |
| dc.subject.other | ABTS radical scavenging assay | |
| dc.subject.other | aerial plant part | |
| dc.subject.other | antioxidant activity | |
| dc.subject.other | Article | |
| dc.subject.other | chelation | |
| dc.subject.other | chemical composition | |
| dc.subject.other | chemical fingerprinting | |
| dc.subject.other | cholinesterase inhibition | |
| dc.subject.other | controlled study | |
| dc.subject.other | cupric reducing antioxidant capacity | |
| dc.subject.other | DPPH radical scavenging assay | |
| dc.subject.other | drug cytotoxicity | |
| dc.subject.other | DU145 cell line | |
| dc.subject.other | electrospray mass spectrometry | |
| dc.subject.other | enzyme inhibition | |
| dc.subject.other | ferric reducing antioxidant power assay | |
| dc.subject.other | human | |
| dc.subject.other | human cell | |
| dc.subject.other | liquid chromatography-mass spectrometry | |
| dc.subject.other | molecular model | |
| dc.subject.other | nonhuman | |
| dc.subject.other | protein protein interaction | |
| dc.subject.other | proton nuclear magnetic resonance | |
| dc.subject.other | quantitative analysis | |
| dc.subject.other | systems pharmacology | |
| dc.subject.other | Tanacetum nitens | |
| dc.subject.other | chemistry | |
| dc.subject.other | dose response | |
| dc.subject.other | drug effect | |
| dc.subject.other | isolation and purification | |
| dc.subject.other | tumor cell line | |
| dc.title | Combining chemical profiles and biological abilities of different extracts from Tanacetum nitens (Boiss. & Noë) Grierson using network pharmacology | |
| dc.type | Article | |
| rdl.citation.openalex | 7 | |
| rdl.citation.scopus | 7 | |
| rdl.department | Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy | |
| rdl.department | Department of Botany, Faculty of Science, University of Khartoum, Khartoum, Sudan | |
| rdl.department | Le Laboratoire Agronomie et Environnement, Université de Lorraine, INRAE, LAE, Nancy, France | |
| rdl.department | Department of Molecular Biology and Genetics, Istanbul AREL University, Istanbul, Turkey | |
| rdl.department | Department of Bioinformatics, Pondicherry University, Pudhucherry, India | |
| rdl.department | Department of Medical Biochemistry, Faculty of Medicine, Harran University, Sanliurfa, Turkey | |
| rdl.department | Sanlıurfa Provincial Directorate of National Education, Sanlıurfa, Turkey | |
| rdl.department | Sason Vocational School, Batman University, Batman, Turkey | |
| rdl.department | Pertek Sakine Genç Vocational School, Munzur University, Pertek, Tunceli, Turkey | |
| rdl.department | Department of Faculty, Faculty of Science, Selcuk University, Konya, Turkey | |
| rdl.oa.status | green | |
| rdl.oa.status | closed | |
| rdl.oa.url | https://hdl.handle.net/20.500.12294/4117 | |
| rdl.scopus.quartile | Q2 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED |
