Detailed Chemical Characterization and Biological Propensities of Malabaila lasiocarpa Extracts: An Endemic Plant to Turkey
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.
Anahtar Kelimeler
- Scopus
- 6
- OpenAlex
- 5
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Zengin, Gokhan | |
| dc.contributor.author | Zheleva-Dimitrova, Dimitrina | |
| dc.contributor.author | Babacan, Ebru Yüce | |
| dc.contributor.author | Polat, Rıdvan | |
| dc.contributor.author | Çakılcıoğlu, Uğur | |
| dc.contributor.author | Sadeer, Nabeelah Bibi | |
| dc.contributor.author | Costa, Emmanoel V. | |
| dc.contributor.author | Mahomoodally, Mohamad Fawzi | |
| dc.contributor.author | Naviglio, Daniele | |
| dc.contributor.author | Gallo, Monica | |
| dc.contributor.author | Montesano, Domenico | |
| dc.contributor.author | Lorenzo, José M. | |
| dc.contributor.author | Gevrenova, Reneta | |
| dc.date.accessioned | 2026-10-28T14:55:52.141300400Z | |
| dc.date.available | 2026-10-28T14:55:52.141300400Z | |
| dc.date.issued | 2022 | |
| dc.description.abstract | 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. | |
| dc.identifier.articlenumber | e202200068 | |
| dc.identifier.doi | 10.1002/cbdv.202200068 | |
| dc.identifier.eissn | 1612-1880 | |
| dc.identifier.issn | 1612-1872 | |
| dc.identifier.issue | 4 | |
| dc.identifier.pmid | 35263005 | |
| dc.identifier.scopus | 2-s2.0-85127121023 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/munzur/2836 | |
| dc.identifier.volume | 19 | |
| dc.identifier.wos | WOS:000772515800001 | |
| 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 | antioxidants | |
| dc.subject | coumarins | |
| dc.subject | enzyme inhibition | |
| dc.subject | Malabaila lasiocarpa | |
| dc.subject | natural agents | |
| dc.subject.other | Acarbose | |
| dc.subject.other | Antioxidants | |
| dc.subject.other | Apiaceae | |
| dc.subject.other | Flavonoids | |
| dc.subject.other | Methylene Chloride | |
| dc.subject.other | Plant Extracts | |
| dc.subject.other | Turkey | |
| dc.subject.other | 3 coumaric acid | |
| dc.subject.other | 3 feruloyl 5 caffeoylquinic acid | |
| dc.subject.other | 3 feruloylquinic acid | |
| dc.subject.other | 3 para coumaroylquinic acid | |
| dc.subject.other | 3,4 dicaffeoylquinic acid | |
| dc.subject.other | 3,5 dicaffeoylquinic acid | |
| dc.subject.other | 4 feruloyl 5 caffeoylquinic acid | |
| dc.subject.other | 4 hydroxybenzoic acid | |
| dc.subject.other | 4 hydroxybenzoic acid hexoside | |
| dc.subject.other | 4 hydroxyphenylacetic acid | |
| dc.subject.other | 4 hydroxyphenylacetic acid hexoside | |
| dc.subject.other | 4,5 dicaffeoylquinic acid | |
| dc.subject.other | 5 feruloylquinic acid | |
| dc.subject.other | 5 para coumaroylquinic acid | |
| dc.subject.other | acetoxycinnamic acid hexoside | |
| dc.subject.other | acetylcholinesterase | |
| dc.subject.other | aloimperatorin | |
| dc.subject.other | alpha glucosidase | |
| dc.subject.other | alpha glucosidase inhibitor | |
| dc.subject.other | amylase | |
| dc.subject.other | amylase inhibitor | |
| dc.subject.other | angelicin | |
| dc.subject.other | antioxidant | |
| dc.subject.other | apigenin | |
| dc.subject.other | apigenin 6 hexosyl 8 pentoside | |
| dc.subject.other | apigenin hexuronide | |
| dc.subject.other | apigetrin | |
| dc.subject.other | astragalin | |
| dc.subject.other | bergapten | |
| dc.subject.other | caffeic acid | |
| dc.subject.other | caffeic acid hexoside | |
| dc.subject.other | chlorogenic(5 caffeoylquinic)acid | |
| dc.subject.other | cholinesterase | |
| dc.subject.other | cholinesterase inhibitor | |
| dc.subject.other | chrysoeriol | |
| dc.subject.other | chrysoeriol hexuronide | |
| dc.subject.other | cirsiliol | |
| dc.subject.other | cirsiliol hexoside | |
| dc.subject.other | coumaric acid | |
| dc.subject.other | coumarin | |
| dc.subject.other | coumarin derivative | |
| dc.subject.other | cynarine | |
| dc.subject.other | dichloromethane | |
| dc.subject.other | enzyme inhibitor | |
| dc.subject.other | esculetin | |
| dc.subject.other | esculin | |
| dc.subject.other | ferulic acid | |
| dc.subject.other | flavonoid | |
| dc.subject.other | furocoumarin | |
| dc.subject.other | galantamine | |
| dc.subject.other | gallic acid | |
| dc.subject.other | gallic acid deoxyhexoside | |
| dc.subject.other | gallic acid hexoside | |
| dc.subject.other | gentisic acid | |
| dc.subject.other | gentisic acid hexoside | |
| dc.subject.other | glycoside | |
| dc.subject.other | herniarin | |
| dc.subject.other | hexane | |
| dc.subject.other | hydroxybenzoic acid | |
| dc.subject.other | isoorientin | |
| dc.subject.other | isopimpinellin | |
| dc.subject.other | isoquercetin | |
| dc.subject.other | isorhamnetin | |
| dc.subject.other | isorhamnetin 3 glucoside | |
| dc.subject.other | isorhamnetin deohyhexoside | |
| dc.subject.other | isorhamnetin deoxyhexosyl hexoside | |
| dc.subject.other | isorhamnetin dideoxyhexoside | |
| dc.subject.other | isorhamnetin dihexoside hexosyl hexoside | |
| dc.subject.other | isorhamnetin pentosyl hexoside | |
| dc.subject.other | isorhamnetin rutinoside | |
| dc.subject.other | isovitexin | |
| dc.subject.other | kaempferol | |
| dc.subject.other | kaempferol 7 deoxyhexoside | |
| dc.subject.other | kaempferol acetylhexoside | |
| dc.subject.other | kaempferol deoxyhexosyl hexoside | |
| dc.subject.other | kaempferol di hexoside hexosyl hexoside | |
| dc.subject.other | kaempferol dideohyhexoside | |
| dc.subject.other | kaempferol pentosyl deoxyhexosylsyl | |
| dc.subject.other | kaempferol pentosyl hexoside | |
| dc.subject.other | kojic acid | |
| dc.subject.other | luteolin | |
| dc.subject.other | luteolin 7 glucoside | |
| dc.subject.other | luteolin deohyhexoside | |
| dc.subject.other | luteolin hexuronide | |
| dc.subject.other | Malabaila lasiocarpa extract | |
| dc.subject.other | marmesin | |
| dc.subject.other | marmesin hexoside | |
| dc.subject.other | methanol | |
| dc.subject.other | methoxsalen | |
| dc.subject.other | monophenol monooxygenase | |
| dc.subject.other | naringenin | |
| dc.subject.other | naringenin 6,8 di hexoside | |
| dc.subject.other | neochlorogenic(3 caffeoylquinic)acid | |
| dc.title | Detailed Chemical Characterization and Biological Propensities of Malabaila lasiocarpa Extracts: An Endemic Plant to Turkey | |
| dc.type | Article | |
| rdl.citation.openalex | 5 | |
| rdl.citation.scopus | 6 | |
| rdl.department | Physiology and Biochemistry Research Laboratory, Department of Biology, Science Faculty, Selcuk University, Campus, Konya, 42130, Turkey | |
| rdl.department | Department of Pharmacognosy, Faculty of Pharmacy, Medical University-Sofia, Bulgaria | |
| rdl.department | Munzur University, Pertek Sakine Genç Vocational School, Tunceli, Pertek, 62500, Turkey | |
| rdl.department | Department of Landscape Architecture, Faculty of Agriculture, Bingol University, 12000, Bingöl, Turkey | |
| rdl.department | Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit, 80837, Mauritius | |
| rdl.department | Department of Chemistry, Federal University of Amazonas (UFAM), Manaus, 69080-900, AM, Brazil | |
| rdl.department | Department of Chemical Sciences, University of Naples Federico II, via Cintia, 4, 80126, Naples, Italy | |
| rdl.department | Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, via Pansini 5, 80131, Naples, Italy | |
| rdl.department | Department of Pharmacy, University of Naples Federico II, Via D. Montesano 49, 80131, Naples, Italy | |
| rdl.department | Centro Tecnológico de la Carne de Galicia, Avd. Galicia No. 4, Parque Tecnológico de Galicia, San Cibrao das Viñas, 32900, Ourense, Spain | |
| rdl.oa.status | closed | |
| rdl.scopus.quartile | Q2 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED |
