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dc.contributor.authorGulçin, İlhami
dc.contributor.authorTaslimi, Parham
dc.contributor.authorAygün, Ayşenur
dc.contributor.authorSadeghian, Nastaran
dc.contributor.authorBastem, Enes
dc.contributor.authorKufrevioglu, Omer Irfan
dc.contributor.authorTurkan, Fikret
dc.contributor.authorŞen, Fatih
dc.date.accessioned2019-05-06T13:11:07Z
dc.date.available2019-05-06T13:11:07Z
dc.date.issued2018-11
dc.identifier.urihttp://hdl.handle.net/11772/1152
dc.description.abstractThe glutathione S-transferase (GST) was purified from fresh blood erythrocytes using affinity column chromatography. Also, alpha-amylase from porcine pancreas and alpha-glycosidase from Saccharomyces cerevisiae were used as target enzymes. In this study, these compounds were tested on alpha-amylase, alpha-glycosidase, and GST enzymes and demonstrated effective inhibitor compounds with K-i values in the range of 8.34-40.78 mu M against GST, and 120.53-892.36 nM against alpha-glycosidase. Additionally, the phenolic molecules were tested for the inhibition of alpha-amylase enzyme which determined effective inhibition profile with IC50 values in the range of 175.01-626.58 nM. Indeed, these molecules can be elective inhibitors of GST, alpha-glycosidase and alpha-amylase enzymes as antidiabetic and antiparasitic agents. (C) 2018 Elsevier B.V. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.ijbiomac.2018.08.001en_US
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_US
dc.subjectAntidiabeticen_US
dc.subjectAntiparasiticen_US
dc.subjectGlutathione S-transferaseen_US
dc.subjectEnzyme inhibitionen_US
dc.titleAntidiabetic and antiparasitic potentials: Inhibition effects of some natural antioxidant compounds on α-glycosidase, α-amylase and human glutathione S-transferase enzymesen_US
dc.typearticleen_US
dc.relation.journalInternational Journal of Biological Macromoleculesen_US
dc.contributor.departmentBartın Üniversitesi, Fen Fakültesi, Biyoteknoloji Bölümüen_US
dc.identifier.volume119en_US
dc.identifier.startpage741en_US
dc.identifier.endpage746en_US


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