Combining chemical profiles and biological abilities of different extracts from Tanacetum nitens (Boiss. & Noë) Grierson using network pharmacology

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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.

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https://rdlopen.rawdatalibrary.net/r/munzur/2066Resmi atıflarda kullanılan kalıcı adres
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https://doi.org/10.1002/ardp.202400194Yayıncı resmi DOI adresi
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AlanDeğerDil
dc.contributor.authorDall'Acqua, Stefano
dc.contributor.authorYagi, Sakina
dc.contributor.authorSut, Stefania
dc.contributor.authorUba, Abdullahi Ibrahim
dc.contributor.authorPonniya, Sathish Kumar M.
dc.contributor.authorKoyuncu, Ismail
dc.contributor.authorToprak, Kenan
dc.contributor.authorBalos, Mehmet Maruf
dc.contributor.authorKaplan, Alevcan
dc.contributor.authorÇakılcıoğlu, Uğur
dc.contributor.authorZengin, Gokhan
dc.date.accessioned2026-10-28T14:54:53.871122145Z
dc.date.available2026-10-28T14:54:53.871122145Z
dc.date.issued2024
dc.description.abstractTanacetum 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.articlenumber2400194
dc.identifier.doi10.1002/ardp.202400194
dc.identifier.eissn1521-4184
dc.identifier.issn0365-6233
dc.identifier.issue9
dc.identifier.pmid38877616
dc.identifier.scopus2-s2.0-85196076146
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2066
dc.identifier.volume357
dc.identifier.wosWOS:001250133500001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofArchiv der Pharmazie
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectantioxidant
dc.subjectcytotoxicity
dc.subjectenzyme inhibition
dc.subjectphytoconstituents
dc.subjectTanacetum nitens
dc.subject.otherAntineoplastic Agents, Phytogenic
dc.subject.otherAntioxidants
dc.subject.otherCell Line, Tumor
dc.subject.otherCell Survival
dc.subject.otherDose-Response Relationship, Drug
dc.subject.otherHumans
dc.subject.otherPhytochemicals
dc.subject.otherPlant Components, Aerial
dc.subject.otherPlant Extracts
dc.subject.otherSolvents
dc.subject.otherTanacetum
dc.subject.otheracetic acid ethyl ester
dc.subject.otheracetylcholinesterase
dc.subject.otheralglucosidase alfa
dc.subject.otheralpha glucosidase
dc.subject.otheramylase
dc.subject.othercholinesterase
dc.subject.otherdichloromethane
dc.subject.otherglucosidase
dc.subject.otherglycoside
dc.subject.otherhexane
dc.subject.otherluteolin
dc.subject.othermethanol
dc.subject.othermonophenol monooxygenase
dc.subject.otherorganic solvent
dc.subject.otherparthenolide
dc.subject.otherphytochemical
dc.subject.otherplant extract
dc.subject.otherquercetin
dc.subject.otherquinic acid
dc.subject.othersitosterol
dc.subject.othertanacetol B
dc.subject.otherTanacetum nitens extract
dc.subject.othertatridin B
dc.subject.otherunclassified drug
dc.subject.otherantineoplastic agent
dc.subject.otherantioxidant
dc.subject.othersolvent
dc.subject.otherABTS radical scavenging assay
dc.subject.otheraerial plant part
dc.subject.otherantioxidant activity
dc.subject.otherArticle
dc.subject.otherchelation
dc.subject.otherchemical composition
dc.subject.otherchemical fingerprinting
dc.subject.othercholinesterase inhibition
dc.subject.othercontrolled study
dc.subject.othercupric reducing antioxidant capacity
dc.subject.otherDPPH radical scavenging assay
dc.subject.otherdrug cytotoxicity
dc.subject.otherDU145 cell line
dc.subject.otherelectrospray mass spectrometry
dc.subject.otherenzyme inhibition
dc.subject.otherferric reducing antioxidant power assay
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.otherliquid chromatography-mass spectrometry
dc.subject.othermolecular model
dc.subject.othernonhuman
dc.subject.otherprotein protein interaction
dc.subject.otherproton nuclear magnetic resonance
dc.subject.otherquantitative analysis
dc.subject.othersystems pharmacology
dc.subject.otherTanacetum nitens
dc.subject.otherchemistry
dc.subject.otherdose response
dc.subject.otherdrug effect
dc.subject.otherisolation and purification
dc.subject.othertumor cell line
dc.titleCombining chemical profiles and biological abilities of different extracts from Tanacetum nitens (Boiss. & Noë) Grierson using network pharmacology
dc.typeArticle
rdl.citation.openalex7
rdl.citation.scopus7
rdl.departmentDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy
rdl.departmentDepartment of Botany, Faculty of Science, University of Khartoum, Khartoum, Sudan
rdl.departmentLe Laboratoire Agronomie et Environnement, Université de Lorraine, INRAE, LAE, Nancy, France
rdl.departmentDepartment of Molecular Biology and Genetics, Istanbul AREL University, Istanbul, Turkey
rdl.departmentDepartment of Bioinformatics, Pondicherry University, Pudhucherry, India
rdl.departmentDepartment of Medical Biochemistry, Faculty of Medicine, Harran University, Sanliurfa, Turkey
rdl.departmentSanlıurfa Provincial Directorate of National Education, Sanlıurfa, Turkey
rdl.departmentSason Vocational School, Batman University, Batman, Turkey
rdl.departmentPertek Sakine Genç Vocational School, Munzur University, Pertek, Tunceli, Turkey
rdl.departmentDepartment of Faculty, Faculty of Science, Selcuk University, Konya, Turkey
rdl.oa.statusgreen
rdl.oa.statusclosed
rdl.oa.urlhttps://hdl.handle.net/20.500.12294/4117
rdl.scopus.quartileQ2
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED