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dc.contributor.authorShirinzadeh, Hanif
dc.contributor.authorDilek, Esra
dc.contributor.authorAlım, Zuhal
dc.date.accessioned2022-04-21T11:29:28Z
dc.date.available2022-04-21T11:29:28Z
dc.date.issued2022en_US
dc.identifier.citationShirinzadeh, H., Dilek, E., & Alım, Z. (2022). Evaluation of Naphthalenylmethylen Hydrazine Derivatives as Potent Inhibitors on, Antiatherogenic Enzymes, Paraoxonase I and Acetylcholinesterase Activities. ChemistrySelect, 7(5). https://doi.org/10.1002/slct.202104489 ‌en_US
dc.identifier.issn2365-6549
dc.identifier.urihttps://doi.org/10.1002/slct.202104489
dc.identifier.urihttps://hdl.handle.net/20.500.12513/4406
dc.description.abstractAcetylcholinesterase (AChE) and paraoxonase 1 (PON1) are two important serum ester hydrolases that have antiatherosclerotic effect by inhibiting the oxidation of lipid peroxides. In addition, AChE inhibitors are target molecules for the treatment of Alzheimer's. Naphthalene derivatives are important molecules in the field of pharmacology due to their wide range of biological activities. In this study, the inhibition effects of naphthalenylmethylen hydrazine derivatives on these two metabolic enzymes were investigated. IC50 values of these molecules were determined in the range of 0.158 mu M to 6.862 mu M against PON1, 0.0214 mu M to 0.675 mu M against AChE. As a result, naphthalenylmethylen hydrazine derivatives had strong inhibition effect on both enzymes. In this context, we hope that the results obtained in this study contribute to the determination of the side effects of current and new naphthalene-based pharmacological compounds to be developed. And also be effective in the synthesis studies of new AChE inhibitors.en_US
dc.description.abstractAcetylcholinesterase (AChE) and paraoxonase 1 (PON1) are two important serum ester hydrolases that have antiatherosclerotic effect by inhibiting the oxidation of lipid peroxides. In addition, AChE inhibitors are target molecules for the treatment of Alzheimer's. Naphthalene derivatives are important molecules in the field of pharmacology due to their wide range of biological activities. In this study, the inhibition effects of naphthalenylmethylen hydrazine derivatives on these two metabolic enzymes were investigated. IC50 values of these molecules were determined in the range of 0.158 mu M to 6.862 mu M against PON1, 0.0214 mu M to 0.675 mu M against AChE. As a result, naphthalenylmethylen hydrazine derivatives had strong inhibition effect on both enzymes. In this context, we hope that the results obtained in this study contribute to the determination of the side effects of current and new naphthalene-based pharmacological compounds to be developed. And also be effective in the synthesis studies of new AChE inhibitors.en_US
dc.language.isoengen_US
dc.publisherWıley-V C H Verlag Gmbhen_US
dc.relation.isversionof10.1002/slct.202104489en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcetylcholinesteraseen_US
dc.subjectAcetylcholinesteraseen_US
dc.subjectEnzymeen_US
dc.subjectEnzymeen_US
dc.subjectInhibitionen_US
dc.subjectInhibitionen_US
dc.subjectNaphthaleneen_US
dc.subjectNaphthaleneen_US
dc.subjectParaoxonase 1en_US
dc.subjectParaoxonase 1en_US
dc.titleEvaluation of Naphthalenylmethylen Hydrazine Derivatives as Potent Inhibitors on, Antiatherogenic Enzymes, Paraoxonase I and Acetylcholinesterase Activitiesen_US
dc.typearticleen_US
dc.relation.journalChemistryselecten_US
dc.contributor.departmentFen Edebiyat Fakültesien_US
dc.contributor.authorIDZuhal Alım / 0000-0003-1977-1756en_US
dc.identifier.volume7en_US
dc.identifier.issue5en_US
dc.identifier.startpage1en_US
dc.identifier.endpage6en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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