Publication:
Analysis of Saponins and Phenolic Compounds as Inhibitors of Α-Carbonic Anhydrase Isoenzymes

dc.authorscopusid6505809121
dc.authorscopusid23027537500
dc.authorscopusid9275226400
dc.authorscopusid7003865150
dc.authorscopusid57194641217
dc.authorscopusid7003998497
dc.authorscopusid7003998497
dc.contributor.authorKoz, Ö.
dc.contributor.authorEkinci, D.
dc.contributor.authorPerrone, A.
dc.contributor.authorPiacente, S.
dc.contributor.authorAlankuş, Ö.
dc.contributor.authorBedir, E.
dc.contributor.authorSupuran, C.T.
dc.date.accessioned2020-06-21T14:06:11Z
dc.date.available2020-06-21T14:06:11Z
dc.date.issued2013
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Koz] Omer, Department of Chemistry, Ege Üniversitesi, Izmir, Turkey; [Ekinci] Deniz, Department of Agricultural Biotechnology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Perrone] Angela, Department of Pharmaceutical Sciences, Università degli Studi di Salerno, Salerno, SA, Italy; [Piacente] Sonia, Department of Pharmaceutical Sciences, Università degli Studi di Salerno, Salerno, SA, Italy; [Alankuş] Özgen, Department of Chemistry, Ege Üniversitesi, Izmir, Turkey; [Bedir] Erdal, Department of Bioengineering, Ege University Faculty of Engineering, Bornova, Izmir, Turkey; [Supuran] Claudiu T., Laboratorio di Chimica Bioinorganica, Università degli Studi di Firenze, Florence, FI, Italyen_US
dc.description.abstractA series of phenolic and saponin type natural products such as quercetin, rutin, catechin, epicatechin, silymarin, trojanoside H, astragaloside IV, astragaloside VIII and astrasieversianin X, were investigated for their inhibitory effects against the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1). We here report inhibitory effects of these compounds against five α-CA isozymes (hCA I, hCA II, bCA III, hCA IV and hCA VI). Most of the phenolic and saponin type compounds inhibited the isoenzymes quite effectively at low micromolar K<inf>I</inf>-s ranging between 0.1 and 4 μM, whereas a few derivatives were ineffective (K<inf>I</inf>-s > 100 μM). The results were remarkable which might lead to design of novel CAIs with a diverse inhibition mechanism compared to sulfonamide/sulfamate inhibitors. © 2013 Informa UK, Ltd.en_US
dc.identifier.doi10.3109/14756366.2011.651464
dc.identifier.endpage417en_US
dc.identifier.issn1475-6366
dc.identifier.issn1475-6374
dc.identifier.issue2en_US
dc.identifier.pmid22299585
dc.identifier.scopus2-s2.0-84891444678
dc.identifier.scopusqualityQ1
dc.identifier.startpage412en_US
dc.identifier.urihttps://doi.org/10.3109/14756366.2011.651464
dc.identifier.volume28en_US
dc.identifier.wosWOS:000314531000027
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherInforma Healthcareen_US
dc.relation.ispartofJournal of Enzyme Inhibition and Medicinal Chemistryen_US
dc.relation.journalJournal of Enzyme Inhibition and Medicinal Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCarbonic Anhydraseen_US
dc.subjectInhibitionen_US
dc.subjectNatural Phenolicsen_US
dc.subjectSaponinsen_US
dc.titleAnalysis of Saponins and Phenolic Compounds as Inhibitors of Α-Carbonic Anhydrase Isoenzymesen_US
dc.typeArticleen_US
dspace.entity.typePublication

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