Enzyme inhibitory function and phytochemical profile of Inula discoidea using in vitro and in silico methods

dc.authorscopusid30067583700
dc.authorscopusid56486842000
dc.authorscopusid57220203137
dc.authorscopusid57115336200
dc.authorscopusid57203682358
dc.authorscopusid56044678500
dc.authorscopusid57192944111
dc.contributor.authorBursal, Ercan
dc.contributor.authorYılmaz, M.A.
dc.contributor.authorİzol, E.
dc.contributor.authorTürkan, F.
dc.contributor.authorAtalar, M.N.
dc.contributor.authorMurahari, M.
dc.contributor.authorAras, A.
dc.date.accessioned2022-09-04T10:27:03Z
dc.date.available2022-09-04T10:27:03Z
dc.date.issued2021
dc.departmentFakülteler, Sağlık Bilimleri Fakültesi, Hemşirelik Bölümüen_US
dc.departmentFakülteler, Sağlık Bilimleri Fakültesi, Hemşirelik Bölümüen_US
dc.description.abstractMany plant species have a large diversity of secondary metabolites with different biological activities. This study aims to assess the phenolic constituent, enzyme inhibitory and antioxidant activities of the aqueous (water) and methanol extracts of Inula discoidea. The enzyme assays showed effective enzyme inhibition of the methanol extract against acetylcholinesterase (AChE), butyrylcholinesterase (BChE), glutathione S-transferase (GST), and ?-glycosidase (?-Gly) enzymes. The IC50 values for AChE, BChE, GST, and ?-Gly were found as 38.5 mg/mL, 34.65 mg/mL, 77.0 mg/mL, and 40.76 mg/mL, respectively. Antioxidant properties of the aqueous and methanol extracts of I. discoidea were determined by four well-known in vitro techniques (ABTS, CUPRAC, DPPH, and FRAP methods). The antioxidant values of both water and methanol extracts were found to be better than the standard antioxidants (BHA, BHT, ascorbic acid, and ?-tocopherol) in ABTS and CUPRAC methods. According to an updated LC-MS/MS technique analysis, quinic acid (21.08 mg/g), protocatechuic acid (4.49 mg/g), and gallic acid (0.48 mg/g) were found as major phenolic compounds of the plant extract. The binding interactions of major phenolic compounds of I. discoidea with the AChE, BChE, GST, and ?-Gly enzymes were investigated by the molecular docking studies. © 2021en_US
dc.description.sponsorship2019-FBE-A13en_US
dc.description.sponsorshipThe authors gratefully acknowledge the financial support from the Iğdır University ( 2019-FBE-A13 ). Also, the authors would like thank to Omer Kilic for the identification of the plant species.en_US
dc.identifier.doi10.1016/j.bpc.2021.106629
dc.identifier.issn0301-4622
dc.identifier.pmid34126547
dc.identifier.scopus2-s2.0-85107703077
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://hdl.handle.net/20.500.12639/4708
dc.identifier.volume277en_US
dc.identifier.wosWOS:000686156800005
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorBursal, Ercan
dc.language.isoen
dc.publisherElsevier B.V.en_US
dc.relation.ispartofBiophysical Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAntioxidanten_US
dc.subjectEnzyme inhibitionen_US
dc.subjectInula discoideaen_US
dc.subjectLC-MS/MSen_US
dc.subjectMolecular dockingen_US
dc.subjectacetylcholinesteraseen_US
dc.subjectantioxidanten_US
dc.subjectapigeninen_US
dc.subjectascorbic aciden_US
dc.subjectbutylated hydroxyanisoleen_US
dc.subjectbutylcresolen_US
dc.subjectchlorogenic aciden_US
dc.subjectcholinesteraseen_US
dc.subjectgallic aciden_US
dc.subjectglutathione transferaseen_US
dc.subjectglycosidaseen_US
dc.subjectInula discoidea extracten_US
dc.subjectluteolinen_US
dc.subjectmethanolen_US
dc.subjectmiquelianinen_US
dc.subjectphenol derivativeen_US
dc.subjectphytochemicalen_US
dc.subjectplant extracten_US
dc.subjectprotocatechualdehydeen_US
dc.subjectprotocatechuic aciden_US
dc.subjectquinic aciden_US
dc.subjectsalicylic aciden_US
dc.subjecttocopherolen_US
dc.subjectunclassified drugen_US
dc.subjectwateren_US
dc.subjectacetylcholinesteraseen_US
dc.subjectcholinesteraseen_US
dc.subjectphytochemicalen_US
dc.subjectABTS radical scavenging assayen_US
dc.subjectantioxidant activityen_US
dc.subjectArticleen_US
dc.subjectcomputer modelen_US
dc.subjectcontrolled studyen_US
dc.subjectDPPH radical scavenging assayen_US
dc.subjectenzyme activityen_US
dc.subjectenzyme assayen_US
dc.subjectenzyme inhibitionen_US
dc.subjectferric reducing antioxidant poweren_US
dc.subjectIC50en_US
dc.subjectin vitro studyen_US
dc.subjectInulaen_US
dc.subjectInula discoideaen_US
dc.subjectliquid chromatography-mass spectrometryen_US
dc.subjectmolecular dockingen_US
dc.subjectnonhumanen_US
dc.subjectInulaen_US
dc.subjectAcetylcholinesteraseen_US
dc.subjectButyrylcholinesteraseen_US
dc.subjectInulaen_US
dc.subjectMolecular Docking Simulationen_US
dc.subjectPhytochemicalsen_US
dc.titleEnzyme inhibitory function and phytochemical profile of Inula discoidea using in vitro and in silico methodsen_US
dc.typeArticle

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