Evaluation of Naphthalenylmethylen Hydrazine Derivatives as Potent Inhibitors on, Antiatherogenic Enzymes, Paraoxonase I and Acetylcholinesterase Activities
Özet
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 μM to 6.862 μM against PON1, 0.0214 μM to 0.675 μM 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. © 2022 Wiley-VCH GmbH
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Shirinzadeh, Hanif | |
| dc.contributor.author | Dilek, Esra | |
| dc.contributor.author | Alım, Zuhal | |
| dc.date.accessioned | 2026-10-18T20:27:40.200485217Z | |
| dc.date.available | 2026-10-18T20:27:40.200485217Z | |
| dc.date.issued | 2022 | |
| 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 μM to 6.862 μM against PON1, 0.0214 μM to 0.675 μM 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. © 2022 Wiley-VCH GmbH | |
| dc.description.sponsorship | . The authors appreciate the Scientific Research Council of Erzincan Binali Yildirim University for their support of the Project (Project No: SAG‐A‐240215‐0120) | |
| dc.identifier.doi | 10.1002/slct.202104489 | |
| dc.identifier.issn | 2365-6549 | |
| dc.identifier.issue | 5 | |
| dc.identifier.scopus | 2-s2.0-85128069293 | |
| dc.identifier.startpage | e202104489 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/12800 | |
| dc.identifier.volume | 7 | |
| dc.identifier.wos | WOS:000750964800005 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Inc | |
| dc.relation.ispartof | ChemistrySelect | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Acetylcholinesterase | |
| dc.subject | Enzyme | |
| dc.subject | Inhibition | |
| dc.subject | Naphthalene | |
| dc.subject | Paraoxonase 1 | |
| dc.subject | HIGH-DENSITY-LIPOPROTEINS | |
| dc.subject | PHARMACOLOGICAL EVALUATION | |
| dc.subject | SERUM PARAOXONASE | |
| dc.subject | VITRO | |
| dc.subject | ATHEROSCLEROSIS | |
| dc.subject | POLYMORPHISM | |
| dc.subject | ANALOGS | |
| dc.subject | DESIGN | |
| dc.subject | SERIES | |
| dc.subject | Chemistry, Multidisciplinary | |
| dc.subject | Chemistry | |
| dc.title | Evaluation of Naphthalenylmethylen Hydrazine Derivatives as Potent Inhibitors on, Antiatherogenic Enzymes, Paraoxonase I and Acetylcholinesterase Activities | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 16 | |
| rdl.citation.wos | 16 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
