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dc.contributor.authorGocer, Hulya
dc.contributor.authorTopal, Fevzi
dc.contributor.authorTopal, Meryem
dc.contributor.authorKucuk, Murat
dc.contributor.authorTeke, Dilek
dc.contributor.authorGulcin, Ilhami
dc.contributor.authorSupuran, Claudiu T.
dc.date.accessioned2021-11-09T19:50:15Z
dc.date.available2021-11-09T19:50:15Z
dc.date.issued2016
dc.identifier.issn1475-6366
dc.identifier.issn1475-6374
dc.identifier.urihttps://doi.org/10.3109/14756366.2015.1036051
dc.identifier.urihttps://hdl.handle.net/20.500.12440/4223
dc.description.abstractTaxifolin, also known as dihydroquercetin, is a flavonoid commonly found in plants. Carbonic anhydrase (CA, EC 4.2.1.1) plays an important role in many critical physiological events including carbon dioxide (CO2)/bicarbonate (HCO3-) respiration and pH regulation. There are 16 known CA isoforms in humans, of which human hCA isoenzymes I and II (hCA I and II) are ubiquitous cytosolic isoforms. In this study, the inhibition properties of taxifolin against the slow cytosolic isoenzyme hCA I, and the ubiquitous and dominant rapid cytosolic isoenzyme hCA II were studied. Taxifolin, as a naturally bioactive flavonoid, has a K-i of 29.2nM against hCA I, and 24.2nM against hCA II. For acetylcholinesterase enzyme (AChE) inhibition, K-i parameter of taxifolin was determined to be 16.7nM. These results clearly show that taxifolin inhibited both CA isoenzymes and AChE at the nM levels.en_US
dc.description.sponsorshipDeanship of Scientific Research at King Saud University through the Research Group Project [RGP-VPP-254]en_US
dc.description.sponsorshipThe authors declare no conflict of interest. I.G. and S.H.A. would like to extend his sincere appreciation to the Deanship of Scientific Research at King Saud University for its funding of this research through the Research Group Project No. RGP-VPP-254.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.ispartofJournal of Enzyme Inhibition and Medicinal Chemistryen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcetylcholinesteraseen_US
dc.subjectcarbonic anhydraseen_US
dc.subjectenzyme inhibitionen_US
dc.subjectenzyme purificationen_US
dc.subjecttaxifolinen_US
dc.titleAcetylcholinesterase and carbonic anhydrase isoenzymes I and II inhibition profiles of taxifolinen_US
dc.typearticleen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.description.wospublicationidWOS:000372017000012en_US
dc.description.scopuspublicationid2-s2.0-84961247798en_US
dc.departmentGümüşhane Üniversitesien_US
dc.authoridGULCIN, Ilhami / 0000-0001-5993-1668
dc.identifier.volume31en_US
dc.identifier.issue3en_US
dc.identifier.startpage441en_US
dc.identifier.doi10.3109/14756366.2015.1036051
dc.identifier.endpage447en_US
dc.authorwosidAlwasel, Saleh / AAD-4023-2019
dc.authorwosidGULCIN, Ilhami / F-1428-2014
dc.authorscopusid54794060500
dc.authorscopusid35811768400
dc.authorscopusid55929192400
dc.authorscopusid20334751800
dc.authorscopusid57186648600
dc.authorscopusid35509141500
dc.authorscopusid29067512200
dc.description.pubmedpublicationidPubMed: 25893707en_US


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