Publication: Carbonic Anhydrase Inhibitory Properties of Some Uracil Derivatives
| dc.authorscopusid | 57190938318 | |
| dc.authorscopusid | 23013520200 | |
| dc.authorscopusid | 7102904152 | |
| dc.authorscopusid | 23027537500 | |
| dc.contributor.author | Türkoǧlu, E. | |
| dc.contributor.author | Şentürk, M. | |
| dc.contributor.author | Supuran, C.T. | |
| dc.contributor.author | Ekinci, D. | |
| dc.date.accessioned | 2020-06-21T13:26:51Z | |
| dc.date.available | 2020-06-21T13:26:51Z | |
| dc.date.issued | 2017 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Türkoǧlu] Emir Alper, Department of Pharmaceutical Technology, Aǧrı İbrahim Çeçen Üniversitesi, Agri, Agri, Turkey; [Şentürk] Murat, Department of Chemistry, Aǧrı İbrahim Çeçen Üniversitesi, Agri, Agri, Turkey; [Supuran] Claudiu T., Laboratorio di Chimica Bioinorganica, Università degli Studi di Firenze, Florence, FI, Italy; [Ekinci] Deniz, Department of Agricultural Biotechnology, Ondokuz Mayis Üniversitesi, Samsun, Turkey | en_US |
| dc.description.abstract | Inhibitors of carbonic anhydrase (CA) have been carried out in many therapeutic applications, especially antiglaucoma activity. In this study, we investigated some uracil derivatives (4–12) to inhibit human CA I (hCA I) and II (hCA II) isoenzymes. The K<inf>I</inf> values of the compounds 4–12 are in the range of 0.085–428 µM for hCA I and of 0.1715–645 µM against hCA II, respectively. It is concluded from the kinetic investigations, all compounds used in the study act as competitive inhibitors with substrate, 4-NPA. Uracil derivatives are emerging agents for the inhibiton of carbonic anhydrase which could be used in biomedicine. © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. | en_US |
| dc.identifier.doi | 10.1080/14756366.2016.1235043 | |
| dc.identifier.endpage | 77 | en_US |
| dc.identifier.issn | 1475-6366 | |
| dc.identifier.issn | 1475-6374 | |
| dc.identifier.issue | 1 | en_US |
| dc.identifier.pmid | 28097897 | |
| dc.identifier.scopus | 2-s2.0-85015599725 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 74 | en_US |
| dc.identifier.uri | https://doi.org/10.1080/14756366.2016.1235043 | |
| dc.identifier.volume | 32 | en_US |
| dc.identifier.wos | WOS:000392591100053 | |
| dc.identifier.wosquality | Q1 | |
| dc.language.iso | en | en_US |
| dc.publisher | Taylor and Francis Ltd healthcare.enquiries@informa.com | en_US |
| dc.relation.ispartof | Journal of Enzyme Inhibition and Medicinal Chemistry | en_US |
| dc.relation.journal | Journal of Enzyme Inhibition and Medicinal Chemistry | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Carbonic Anhydrase | en_US |
| dc.subject | Hydroxyl | en_US |
| dc.subject | Inhibitor | en_US |
| dc.subject | Uracil Derivatives | en_US |
| dc.title | Carbonic Anhydrase Inhibitory Properties of Some Uracil Derivatives | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
