Screening of Chemical Profile by LC–MS/MS and Assessment of Biological Properties of Achillea sintenisii Hub. Mor. From Turkey

MakaleAçık Erişim
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

The aim of this study was to determine the secondary metabolites of the n-hexane, ethyl acetate, methanol, and water extracts of Achillea sintenisii Hub. Mor. and to ascertain their divergent biological properties. LC–MS/MS analysis was performed to identify the bioactive compounds. The anticancer properties of the samples were tested against human breast (MCF-7 and MDA-MB-453) and colon (HT-29) cancer cell lines by XTT assay. The anti-Alzheimer's studies were performed using Ellman's assay. The antimicrobial studies were carried out by Kirby–Bauer disc diffusion method. The antioxidative potential of the samples was evaluated on the basis of 2,2-diphenyl-1-picrylhydrazyl scavenging and ferric reducing antioxidant power assays, LC–MS/MS analysis revealed 27 phytochemicals, including high concentrations of quinic acid, gentisic acid, chlorogenic acid, luteolin, cynaroside, and caffeic acid. Ethyl acetate extract exhibited the most potent cytoxicity against MDA-MB-453 cells, with an IC50 value of 83.05 µg/mL. All extracts showed stronger inhibitory activity against acetylcholinesterase and butyrylcholinesterase compared to tacrine. The n-hexane, ethyl acetate, and methanol extracts exhibited considerable antimicrobial activity against Enterococcus faecalis, approaching the level of vancomycin. Methanol extract possessed the highest DPPH scavenging and ferric reducing antioxidant power. These findings render A, sintenisii a promising source for the pharmaceutical, cosmetic, and food industries.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/12498Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/cbdv.202500026Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKöksal, Ekrem
dc.contributor.authorAltay, Ahmet
dc.contributor.authorAltın, Sevgi
dc.contributor.authorAlp, Cemalettin
dc.contributor.authorUlutaş, Yakup
dc.contributor.authorŞimşek, Samed
dc.contributor.authorKarakuş, Sinem
dc.contributor.authorAkyüz, Sümeyye
dc.contributor.authorAygül, İmdat
dc.contributor.authorAkşit, Hüseyin
dc.contributor.authorYilmaz, Mustafa Abdullah
dc.date.accessioned2026-10-22T10:20:11.390744685Z
dc.date.available2026-10-22T10:20:11.390744685Z
dc.date.issued2025
dc.description.abstractThe aim of this study was to determine the secondary metabolites of the n-hexane, ethyl acetate, methanol, and water extracts of Achillea sintenisii Hub. Mor. and to ascertain their divergent biological properties. LC–MS/MS analysis was performed to identify the bioactive compounds. The anticancer properties of the samples were tested against human breast (MCF-7 and MDA-MB-453) and colon (HT-29) cancer cell lines by XTT assay. The anti-Alzheimer's studies were performed using Ellman's assay. The antimicrobial studies were carried out by Kirby–Bauer disc diffusion method. The antioxidative potential of the samples was evaluated on the basis of 2,2-diphenyl-1-picrylhydrazyl scavenging and ferric reducing antioxidant power assays, LC–MS/MS analysis revealed 27 phytochemicals, including high concentrations of quinic acid, gentisic acid, chlorogenic acid, luteolin, cynaroside, and caffeic acid. Ethyl acetate extract exhibited the most potent cytoxicity against MDA-MB-453 cells, with an IC50 value of 83.05 µg/mL. All extracts showed stronger inhibitory activity against acetylcholinesterase and butyrylcholinesterase compared to tacrine. The n-hexane, ethyl acetate, and methanol extracts exhibited considerable antimicrobial activity against Enterococcus faecalis, approaching the level of vancomycin. Methanol extract possessed the highest DPPH scavenging and ferric reducing antioxidant power. These findings render A, sintenisii a promising source for the pharmaceutical, cosmetic, and food industries.
dc.description.sponsorshipTürkiye Bilimsel ve Teknolojik Araştırma Kurumu, TUBITAK, (119Z718)
dc.description.sponsorshipTürkiye Bilimsel ve Teknolojik Araştırma Kurumu, TUBITAK
dc.identifier.articlenumbere202500026
dc.identifier.doi10.1002/cbdv.202500026
dc.identifier.eissn1612-1880
dc.identifier.issn1612-1872
dc.identifier.issue7
dc.identifier.pmid40012270
dc.identifier.scopus2-s2.0-85219586770
dc.identifier.startpagee202500026
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/12498
dc.identifier.volume22
dc.identifier.wosWOS:001433602500001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofChemistry and Biodiversity
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAchillea sintenisii Hub. Mor
dc.subjectbiological activity
dc.subjectseconder metabolites
dc.subject.classificationBiochemistry & Molecular Biology
dc.subject.classificationChemistry, Multidisciplinary
dc.subject.classificationChemistry
dc.subject.otherAcetylcholinesterase
dc.subject.otherAchillea
dc.subject.otherAnti-Bacterial Agents
dc.subject.otherAntineoplastic Agents, Phytogenic
dc.subject.otherAntioxidants
dc.subject.otherBiphenyl Compounds
dc.subject.otherCell Line, Tumor
dc.subject.otherCell Proliferation
dc.subject.otherCell Survival
dc.subject.otherCholinesterase Inhibitors
dc.subject.otherChromatography, Liquid
dc.subject.otherDose-Response Relationship, Drug
dc.subject.otherDrug Screening Assays, Antitumor
dc.subject.otherHumans
dc.subject.otherLiquid Chromatography-Mass Spectrometry
dc.subject.otherMicrobial Sensitivity Tests
dc.subject.otherPicrates
dc.subject.otherPlant Extracts
dc.subject.otherTandem Mass Spectrometry
dc.subject.otherTurkey
dc.subject.other4 oh benzoic acid
dc.subject.otheracacetin
dc.subject.otheracetic acid ethyl ester
dc.subject.otherachillea sintenisii extract
dc.subject.otheraconitic acid
dc.subject.otheramentoflavone
dc.subject.otherantibiotic agent
dc.subject.otherantifungal agent
dc.subject.otherantineoplastic agent
dc.subject.otherantioxidant
dc.subject.otherapigenin
dc.subject.otherastragalin
dc.subject.othercaffeic acid
dc.subject.othercatechin
dc.subject.otherchlorogenic acid
dc.subject.othercholinesterase
dc.subject.otherchrysin
dc.subject.othercosmosiin
dc.subject.othercoumaric acid
dc.subject.othercoumarin
dc.subject.othercynarine
dc.subject.otherdaidzein
dc.subject.otherdaidzin
dc.subject.otherellagic acid
dc.subject.otherepicatechin
dc.subject.otherepicatechin gallate
dc.subject.otherepigallacatechin
dc.subject.otherepigallocatechin gallate
dc.subject.othererythromycin
dc.subject.otherferulic acid
dc.subject.otherfisetin
dc.subject.otherfumaric acid
dc.subject.othergallic acid
dc.subject.othergenistein
dc.subject.othergenistin
dc.subject.othergentisic acid
dc.subject.otherhesperetin
dc.subject.otherhesperidin
dc.subject.otherhexane
dc.subject.otherisoquercetin
dc.subject.otherkaempferol
dc.subject.otherluteolin
dc.subject.otherluteolin 7 glucoside
dc.subject.othermethanol
dc.subject.othermiquelianin
dc.subject.othernaringenin
dc.subject.othernicotiflorin
dc.subject.othernootropic agent
dc.subject.otherpara coumaric acid
dc.subject.otherpiceid
dc.subject.otherplant extract
dc.subject.otherprotocatechualdehyde
dc.subject.otherprotocatechuic acid
dc.subject.otherquercetin
dc.subject.otherquercitrin
dc.subject.otherquinic acid
dc.subject.otherreactive oxygen metabolite
dc.subject.otherrosmarinic acid
dc.subject.otherrutoside
dc.subject.othersalicylic acid
dc.subject.othersinapic acid
dc.subject.othersyringic acid
dc.subject.othersyringic aldehyde
dc.subject.othertannin
dc.subject.othertrolox C
dc.subject.otherunclassified drug
dc.subject.othervancomycin
dc.subject.othervanilic acid
dc.subject.othervanillin
dc.subject.otherwater
dc.subject.other1,1-diphenyl-2-picrylhydrazyl
dc.subject.otherantiinfective agent
dc.subject.otherbiphenyl derivative
dc.subject.othercholinesterase inhibitor
dc.subject.otherpicric acid
dc.subject.otherAchillea sintenisii hub mor
dc.subject.otheraerial plant part
dc.subject.otherAlzheimer disease
dc.subject.otherantibacterial activity
dc.subject.otherantifungal activity
dc.titleScreening of Chemical Profile by LC–MS/MS and Assessment of Biological Properties of Achillea sintenisii Hub. Mor. From Turkey
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex11
rdl.citation.scopus10
rdl.citation.wos8
rdl.departmentDepartment of Nutrition and Dietetics, Faculty of Health Sciences, Gümüşhane University, Gümüşhane, Turkey
rdl.oa.statusgreen
rdl.oa.statuspreprint
rdl.oa.urlhttps://pubmed.ncbi.nlm.nih.gov/40012270/
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)