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dc.contributor.authorCaglayan, C. and Gulcin, İ.
dc.date.accessioned2021-04-08T12:07:40Z
dc.date.available2021-04-08T12:07:40Z
dc.date.issued2018
dc.identifier10.1002/jbt.22010
dc.identifier.issn10956670
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85040674777&doi=10.1002%2fjbt.22010&partnerID=40&md5=a3163aa59bc62660a50e15c4fbb22f49
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4406
dc.description.abstractAvermectins are used worldwide as antiparasitic drugs in the field of veterinary medicine and as agricultural pesticides and insecticides. Carbonic anhydrase (CA, E.C. 4.2.1.1) is a zinc-containing metalloenzyme that catalyzes the reversible hydration of carbon dioxide (CO2) to yield protons (H+) and bicarbonate (HCO3 −). In this study, some avermectins, including abamectin, doramectin, eprinomectin, and moxidectin, were investigated for in vitro inhibitory effects on the CA enzyme purified from goat liver, which was purified (125.00-fold) using sepharose 4B-l-tyrosine-sulfanilamide affinity chromatography, with a yield of 68.27% and a specific activity of 21765.31 EU/mg proteins. The inhibition results obtained from this study showed Ki values of 0.283, 0.153, 0.232, and 0.317 nM for abamectin, doramectin, eprinomectin, and moxidectin, respectively. On the other hand, acetazolamide, well-known clinically established CA inhibitor, possessed a Ki value of 0.707 nM against goat liver CA. © 2017 Wiley Periodicals, Inc.
dc.language.isoEnglish
dc.sourceJournal of Biochemical and Molecular Toxicology
dc.titleThe toxicological effects of some avermectins on goat liver carbonic anhydrase enzyme


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