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dc.contributor.authorKoz, Omer
dc.contributor.authorEkinci, Deniz
dc.contributor.authorPerrone, Angela
dc.contributor.authorPiacente, Sonia
dc.contributor.authorAlankus-Caliskan, Ozgen
dc.contributor.authorBedir, Erdal
dc.contributor.authorSupuran, Claudiu T.
dc.date.accessioned2020-06-21T14:06:11Z
dc.date.available2020-06-21T14:06:11Z
dc.date.issued2013
dc.identifier.issn1475-6366
dc.identifier.issn1475-6374
dc.identifier.urihttps://doi.org/10.3109/14756366.2011.651464
dc.identifier.urihttps://hdl.handle.net/20.500.12712/15928
dc.descriptionKOZ, OMER/0000-0002-2882-6811; Bedir, Erdal/0000-0003-1262-063Xen_US
dc.descriptionWOS: 000314531000027en_US
dc.descriptionPubMed: 22299585en_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 alpha-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-i-s ranging between 0.1 and 4 mu M, whereas a few derivatives were ineffective (K-i-s > 100 mu M). The results were remarkable which might lead to design of novel CAIs with a diverse inhibition mechanism compared to sulfonamide/sulfamate inhibitors.en_US
dc.description.sponsorshipFP7 EU grant (Metoxia)European Union (EU)en_US
dc.description.sponsorshipThis study was financed by an FP7 EU grant (Metoxia) to CTS.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.isversionof10.3109/14756366.2011.651464en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_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 alpha-carbonic anhydrase isoenzymesen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume28en_US
dc.identifier.issue2en_US
dc.identifier.startpage412en_US
dc.identifier.endpage417en_US
dc.relation.journalJournal of Enzyme Inhibition and Medicinal Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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