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dc.contributor.authorTaslimi, P. and Kocyigit, U.M. and Tüzün, B. and Kirici, M.
dc.date.accessioned2021-04-08T12:06:35Z
dc.date.available2021-04-08T12:06:35Z
dc.date.issued2020
dc.identifier10.1080/07391102.2020.1840440
dc.identifier.issn07391102
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85095731468&doi=10.1080%2f07391102.2020.1840440&partnerID=40&md5=fb5abf24c83fbd29c12ea3b53db76fdf
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4002
dc.description.abstractGallocatechin gallate is a form of catechin and an ester of gallocatechin and gallic acid. This is an epimer of the gallate epigallocatechin. In this study, the effect of this molecule, containing a biologically active group, was investigated in terms of important metabolic enzymes (carbonic anhydrase isoenzymes I and II (hCA I and II), achethylcholinesterase (AChE) and α-glycosidase (α-Gly) enzymes). The molecular docking method used to compare the biological activities of the Catechin 5-O-gallate molecule against enzymes was used. Afterwards, the ADME/T analysis was performed to investigate the drug availability of the Catechin 5-O-gallate molecule and the parameters obtained from ADME/T analysis were examined. Continuation of this study, for evaluating antioxidant and radical scavenging capacity Catechin 5-O-gallate, cupric ion (Cu2+) reduction capacity by CUPRAC method, Fe3+-Fe2+ reducing capacity, DPPH free radical clarifying (DPPH·), ABTS radical clarifying (ABTS•+) were performed separately and during the study, trolox, α-tocopherol BHT and BHA were used as the reference antioxidant compound. Comparisons were applied with the four standard substances. Communicated by Ramaswamy H. Sarma. © 2020 Informa UK Limited, trading as Taylor & Francis Group.
dc.language.isoEnglish
dc.sourceJournal of Biomolecular Structure and Dynamics
dc.titleBiological effects and molecular docking studies of Catechin 5-O-gallate: antioxidant, anticholinergics, antiepileptic and antidiabetic potentials


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