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dc.contributor.authorParham, Taslimi
dc.contributor.authorSabiya, Osmanova
dc.contributor.authorIlhami, Gulcin
dc.contributor.authorSabira, Sardarova
dc.contributor.authorVagif, Farzaliyev
dc.contributor.authorAfsun, Sujayev
dc.contributor.authorRuya, Kaya
dc.contributor.authorFatma, Koc
dc.contributor.authorSukru, Beydemir
dc.contributor.authorSaleh H., Alwasel
dc.contributor.authorOmer Irfan, Kufrevioglu
dc.date.accessioned2019-05-17T08:13:25Z
dc.date.available2019-05-17T08:13:25Z
dc.date.issued2017-09
dc.identifier.urihttp://hdl.handle.net/11772/1195
dc.description.abstractCompounds containing nitrogen and sulfur atoms can be widely used in various fields, including industry, medicine, biotechnology, and chemical technology. Among them, amides of acids and heterocyclic compounds have an important place. These amides and thiazolidine-4-ones showed good inhibitory action against butyrylcholinesterase (BChE), acetylcholinesterase (AChE), and human carbonic anhydrase isoforms. AChE exists at high concentrations in the brain and red blood cells. BChE is an important enzyme that is plentiful in the liver, and it is released into the blood in a soluble form. They were demonstrated to have effective inhibition profiles with K-i values of 23.76-102.75nM against hCA I, 58.92-136.64nM against hCA II, 1.40-12.86nM against AChE, and 9.82-52.77nM against BChE. On the other hand, acetazolamide showed K-i value of 482.63 +/- 56.20nM against hCA I, and 1019.60 +/- 163.70nM against hCA II. Additionally, Tacrine inhibited AChE and BChE, showing K-i values of 397.03 +/- 31.66 and 210.21 +/- 15.98nM, respectively.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/jbt.21931en_US
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_US
dc.subjectAcetophenoneen_US
dc.subjectAcetylcholinesteraseen_US
dc.subjectButyrylcholinesteraseen_US
dc.subjectCarbonic anhydraseen_US
dc.subjectEnzyme inhibitionen_US
dc.titleDiscovery of potent carbonic anhydrase, acetylcholinesterase, and butyrylcholinesterase enzymes inhibitors: The new amides and thiazolidine-4-ones synthesized on an acetophenone baseen_US
dc.typearticleen_US
dc.relation.journalJournal of Biochemical and Molecular Toxicologyen_US
dc.contributor.departmentBartın Üniversitesi, Fen Fakültesi, Biyoteknoloji Bölümüen_US
dc.identifier.volume31en_US
dc.identifier.issue9en_US
dc.identifier.startpagee21931en_US


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