Detailed Chemical Characterization and Biological Propensities of Malabaila lasiocarpa Extracts: An Endemic Plant to Turkey

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Özet

This study focused on the biological evaluation and chemical characterization of Malabaila lasiocarpa Boiss. (M. lasiocarpa) (Family: Apiaceae). The phytochemical profile, antioxidant, enzyme inhibitory of the methanolic, aqueous, dichloromethane, hexane extracts were investigated. Based on UHPLC-HRMS analyses, a total of 101 peaks were annotated or identified for the first time in M. lasiocarpa extracts. They include hydroxybenzoic, hydroxycinnamic, acylquinic acids and their glycosides, C- and O-glycosyl and O-diglycosyl flavonoids. In addition, 10 simple mono- and disubstituted coumarins together with 10 furanocoumarins were tentatively annotated. The methanolic extract possessing the highest phenolic (24.36±0.60 mg gallic acid equivalent/g extract) and flavonoid (69.15±0.37 mg rutin equivalent/g extract) content also exhibited the strongest radical scavenging potential against 2,2-diphenyl-1 picrylhydrazyl (21.73±0.42 mg Trolox equivalent/g extract, respectively), and highest reducing capacity (57.81±0.97 and 28.00±0.40 mg Trolox equivalent/g extract, for cupric reducing antioxidant capacity and ferric reducing antioxidant power, respectively). The dichloromethane extract substantially depressed the tyrosinase (73.92±5.37 mg kojic acid equivalent/g extract), α-amylase (0.63±0.01 mmol acarbose equivalent/g extract) and α-glucosidase (0.69±0.02 mmol acarbose equivalent/g extract) enzymes. This study has produced critical scientific data on M. lasiocarpa which are potential contenders for the development of novel phyto-pharmaceuticals.

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https://doi.org/10.1002/cbdv.202200068Yayıncı resmi DOI adresi
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dc.contributor.authorZengin, Gokhan
dc.contributor.authorZheleva-Dimitrova, Dimitrina
dc.contributor.authorBabacan, Ebru Yüce
dc.contributor.authorPolat, Rıdvan
dc.contributor.authorÇakılcıoğlu, Uğur
dc.contributor.authorSadeer, Nabeelah Bibi
dc.contributor.authorCosta, Emmanoel V.
dc.contributor.authorMahomoodally, Mohamad Fawzi
dc.contributor.authorNaviglio, Daniele
dc.contributor.authorGallo, Monica
dc.contributor.authorMontesano, Domenico
dc.contributor.authorLorenzo, José M.
dc.contributor.authorGevrenova, Reneta
dc.date.accessioned2026-10-28T14:55:52.141300400Z
dc.date.available2026-10-28T14:55:52.141300400Z
dc.date.issued2022
dc.description.abstractThis study focused on the biological evaluation and chemical characterization of Malabaila lasiocarpa Boiss. (M. lasiocarpa) (Family: Apiaceae). The phytochemical profile, antioxidant, enzyme inhibitory of the methanolic, aqueous, dichloromethane, hexane extracts were investigated. Based on UHPLC-HRMS analyses, a total of 101 peaks were annotated or identified for the first time in M. lasiocarpa extracts. They include hydroxybenzoic, hydroxycinnamic, acylquinic acids and their glycosides, C- and O-glycosyl and O-diglycosyl flavonoids. In addition, 10 simple mono- and disubstituted coumarins together with 10 furanocoumarins were tentatively annotated. The methanolic extract possessing the highest phenolic (24.36±0.60 mg gallic acid equivalent/g extract) and flavonoid (69.15±0.37 mg rutin equivalent/g extract) content also exhibited the strongest radical scavenging potential against 2,2-diphenyl-1 picrylhydrazyl (21.73±0.42 mg Trolox equivalent/g extract, respectively), and highest reducing capacity (57.81±0.97 and 28.00±0.40 mg Trolox equivalent/g extract, for cupric reducing antioxidant capacity and ferric reducing antioxidant power, respectively). The dichloromethane extract substantially depressed the tyrosinase (73.92±5.37 mg kojic acid equivalent/g extract), α-amylase (0.63±0.01 mmol acarbose equivalent/g extract) and α-glucosidase (0.69±0.02 mmol acarbose equivalent/g extract) enzymes. This study has produced critical scientific data on M. lasiocarpa which are potential contenders for the development of novel phyto-pharmaceuticals.
dc.identifier.articlenumbere202200068
dc.identifier.doi10.1002/cbdv.202200068
dc.identifier.eissn1612-1880
dc.identifier.issn1612-1872
dc.identifier.issue4
dc.identifier.pmid35263005
dc.identifier.scopus2-s2.0-85127121023
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2836
dc.identifier.volume19
dc.identifier.wosWOS:000772515800001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofChemistry and Biodiversity
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectantioxidants
dc.subjectcoumarins
dc.subjectenzyme inhibition
dc.subjectMalabaila lasiocarpa
dc.subjectnatural agents
dc.subject.otherAcarbose
dc.subject.otherAntioxidants
dc.subject.otherApiaceae
dc.subject.otherFlavonoids
dc.subject.otherMethylene Chloride
dc.subject.otherPlant Extracts
dc.subject.otherTurkey
dc.subject.other3 coumaric acid
dc.subject.other3 feruloyl 5 caffeoylquinic acid
dc.subject.other3 feruloylquinic acid
dc.subject.other3 para coumaroylquinic acid
dc.subject.other3,4 dicaffeoylquinic acid
dc.subject.other3,5 dicaffeoylquinic acid
dc.subject.other4 feruloyl 5 caffeoylquinic acid
dc.subject.other4 hydroxybenzoic acid
dc.subject.other4 hydroxybenzoic acid hexoside
dc.subject.other4 hydroxyphenylacetic acid
dc.subject.other4 hydroxyphenylacetic acid hexoside
dc.subject.other4,5 dicaffeoylquinic acid
dc.subject.other5 feruloylquinic acid
dc.subject.other5 para coumaroylquinic acid
dc.subject.otheracetoxycinnamic acid hexoside
dc.subject.otheracetylcholinesterase
dc.subject.otheraloimperatorin
dc.subject.otheralpha glucosidase
dc.subject.otheralpha glucosidase inhibitor
dc.subject.otheramylase
dc.subject.otheramylase inhibitor
dc.subject.otherangelicin
dc.subject.otherantioxidant
dc.subject.otherapigenin
dc.subject.otherapigenin 6 hexosyl 8 pentoside
dc.subject.otherapigenin hexuronide
dc.subject.otherapigetrin
dc.subject.otherastragalin
dc.subject.otherbergapten
dc.subject.othercaffeic acid
dc.subject.othercaffeic acid hexoside
dc.subject.otherchlorogenic(5 caffeoylquinic)acid
dc.subject.othercholinesterase
dc.subject.othercholinesterase inhibitor
dc.subject.otherchrysoeriol
dc.subject.otherchrysoeriol hexuronide
dc.subject.othercirsiliol
dc.subject.othercirsiliol hexoside
dc.subject.othercoumaric acid
dc.subject.othercoumarin
dc.subject.othercoumarin derivative
dc.subject.othercynarine
dc.subject.otherdichloromethane
dc.subject.otherenzyme inhibitor
dc.subject.otheresculetin
dc.subject.otheresculin
dc.subject.otherferulic acid
dc.subject.otherflavonoid
dc.subject.otherfurocoumarin
dc.subject.othergalantamine
dc.subject.othergallic acid
dc.subject.othergallic acid deoxyhexoside
dc.subject.othergallic acid hexoside
dc.subject.othergentisic acid
dc.subject.othergentisic acid hexoside
dc.subject.otherglycoside
dc.subject.otherherniarin
dc.subject.otherhexane
dc.subject.otherhydroxybenzoic acid
dc.subject.otherisoorientin
dc.subject.otherisopimpinellin
dc.subject.otherisoquercetin
dc.subject.otherisorhamnetin
dc.subject.otherisorhamnetin 3 glucoside
dc.subject.otherisorhamnetin deohyhexoside
dc.subject.otherisorhamnetin deoxyhexosyl hexoside
dc.subject.otherisorhamnetin dideoxyhexoside
dc.subject.otherisorhamnetin dihexoside hexosyl hexoside
dc.subject.otherisorhamnetin pentosyl hexoside
dc.subject.otherisorhamnetin rutinoside
dc.subject.otherisovitexin
dc.subject.otherkaempferol
dc.subject.otherkaempferol 7 deoxyhexoside
dc.subject.otherkaempferol acetylhexoside
dc.subject.otherkaempferol deoxyhexosyl hexoside
dc.subject.otherkaempferol di hexoside hexosyl hexoside
dc.subject.otherkaempferol dideohyhexoside
dc.subject.otherkaempferol pentosyl deoxyhexosylsyl
dc.subject.otherkaempferol pentosyl hexoside
dc.subject.otherkojic acid
dc.subject.otherluteolin
dc.subject.otherluteolin 7 glucoside
dc.subject.otherluteolin deohyhexoside
dc.subject.otherluteolin hexuronide
dc.subject.otherMalabaila lasiocarpa extract
dc.subject.othermarmesin
dc.subject.othermarmesin hexoside
dc.subject.othermethanol
dc.subject.othermethoxsalen
dc.subject.othermonophenol monooxygenase
dc.subject.othernaringenin
dc.subject.othernaringenin 6,8 di hexoside
dc.subject.otherneochlorogenic(3 caffeoylquinic)acid
dc.titleDetailed Chemical Characterization and Biological Propensities of Malabaila lasiocarpa Extracts: An Endemic Plant to Turkey
dc.typeArticle
rdl.citation.openalex5
rdl.citation.scopus6
rdl.departmentPhysiology and Biochemistry Research Laboratory, Department of Biology, Science Faculty, Selcuk University, Campus, Konya, 42130, Turkey
rdl.departmentDepartment of Pharmacognosy, Faculty of Pharmacy, Medical University-Sofia, Bulgaria
rdl.departmentMunzur University, Pertek Sakine Genç Vocational School, Tunceli, Pertek, 62500, Turkey
rdl.departmentDepartment of Landscape Architecture, Faculty of Agriculture, Bingol University, 12000, Bingöl, Turkey
rdl.departmentDepartment of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit, 80837, Mauritius
rdl.departmentDepartment of Chemistry, Federal University of Amazonas (UFAM), Manaus, 69080-900, AM, Brazil
rdl.departmentDepartment of Chemical Sciences, University of Naples Federico II, via Cintia, 4, 80126, Naples, Italy
rdl.departmentDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, via Pansini 5, 80131, Naples, Italy
rdl.departmentDepartment of Pharmacy, University of Naples Federico II, Via D. Montesano 49, 80131, Naples, Italy
rdl.departmentCentro Tecnológico de la Carne de Galicia, Avd. Galicia No. 4, Parque Tecnológico de Galicia, San Cibrao das Viñas, 32900, Ourense, Spain
rdl.oa.statusclosed
rdl.scopus.quartileQ2
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED