dc.contributor.author | Shirinzadeh, Hanif | |
dc.contributor.author | Dilek, Esra | |
dc.contributor.author | Alım, Zuhal | |
dc.date.accessioned | 2022-04-21T11:29:28Z | |
dc.date.available | 2022-04-21T11:29:28Z | |
dc.date.issued | 2022 | en_US |
dc.identifier.citation | Shirinzadeh, 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.issn | 2365-6549 | |
dc.identifier.uri | https://doi.org/10.1002/slct.202104489 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12513/4406 | |
dc.description.abstract | Acetylcholinesterase (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.abstract | Acetylcholinesterase (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.iso | eng | en_US |
dc.publisher | Wıley-V C H Verlag Gmbh | en_US |
dc.relation.isversionof | 10.1002/slct.202104489 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Acetylcholinesterase | en_US |
dc.subject | Acetylcholinesterase | en_US |
dc.subject | Enzyme | en_US |
dc.subject | Enzyme | en_US |
dc.subject | Inhibition | en_US |
dc.subject | Inhibition | en_US |
dc.subject | Naphthalene | en_US |
dc.subject | Naphthalene | en_US |
dc.subject | Paraoxonase 1 | en_US |
dc.subject | Paraoxonase 1 | en_US |
dc.title | Evaluation of Naphthalenylmethylen Hydrazine Derivatives as Potent Inhibitors on, Antiatherogenic Enzymes, Paraoxonase I and Acetylcholinesterase Activities | en_US |
dc.type | article | en_US |
dc.relation.journal | Chemistryselect | en_US |
dc.contributor.department | Fen Edebiyat Fakültesi | en_US |
dc.contributor.authorID | Zuhal Alım / 0000-0003-1977-1756 | en_US |
dc.identifier.volume | 7 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.startpage | 1 | en_US |
dc.identifier.endpage | 6 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |