Development of pyridazinone derivatives linked ethyl-bridged-1,2,4-triazole for potential cancer therapy
| dc.contributor.author | Merde, Irem Bozbey | |
| dc.contributor.author | Aykac, Okan | |
| dc.contributor.author | Hepokur, Ceylan | |
| dc.contributor.author | Yasa, Yaren Zisa | |
| dc.contributor.author | Onel, Gulce Taskor | |
| dc.contributor.author | Turkmenoglu, Burcin | |
| dc.date.accessioned | 2026-04-04T13:34:53Z | |
| dc.date.available | 2026-04-04T13:34:53Z | |
| dc.date.issued | 2026 | |
| dc.department | İnönü Üniversitesi | |
| dc.description.abstract | A series of novel pyridazinone derivatives linked ethyl-bridged-1,2,4-triazole were synthesized starting from pchloroacetophenone. The chemical structures of the compounds 5(a-f) were identified by 1HNMR , 13CNMR and LC-QTOF-MS analysis. In this study, the DDPH method was used to evaluate the antioxidant properties of the compounds. The anticancer activity of the compounds was investigated by MTT method in MCF-7, MDA-MB-231 and L929 cell lines. Gene expression levels of Bcl2, Bax and Casp9 genes were compared, and stages of cell death were determined with high accuracy by flow cytometry. Since compound 5a showed promising cytotoxic effects, molecular docking study was performed to support these results and binding values against Bcl2 anti-apoptotic (PDB ID: 6QGG), Bcl-2 (PDB ID: 4IEH) and tubulin regulation (PDB ID: 1SA0) targets were calculated. | |
| dc.description.sponsorship | Scientific and Technological Research Council of Turkey (TUEBITAK 2209-A) [1919B012111441] | |
| dc.description.sponsorship | This study was funded by grants from The Scientific and Technological Research Council of Turkey (TUEBITAK 2209-A) (1919B012111441). | |
| dc.identifier.doi | 10.1016/j.molstruc.2025.143827 | |
| dc.identifier.issn | 0022-2860 | |
| dc.identifier.issn | 1872-8014 | |
| dc.identifier.orcid | 0000-0002-5770-0847 | |
| dc.identifier.orcid | 0000-0002-7363-8801 | |
| dc.identifier.orcid | 0000-0002-9290-938X | |
| dc.identifier.orcid | 0009-0000-7732-2428 | |
| dc.identifier.orcid | 0000-0001-6397-1291 | |
| dc.identifier.orcid | 0000-0002-9375-2329 | |
| dc.identifier.scopus | 2-s2.0-105014928109 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.uri | https://doi.org/10.1016/j.molstruc.2025.143827 | |
| dc.identifier.uri | https://hdl.handle.net/11616/109478 | |
| dc.identifier.volume | 1349 | |
| dc.identifier.wos | WOS:001569350500005 | |
| dc.identifier.wosquality | Q2 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | |
| dc.relation.ispartof | Journal of Molecular Structure | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WOS_20250329 | |
| dc.subject | Anticancer activity | |
| dc.subject | Pyridazinone derivatives | |
| dc.subject | Molecular docking | |
| dc.subject | Triazole | |
| dc.title | Development of pyridazinone derivatives linked ethyl-bridged-1,2,4-triazole for potential cancer therapy | |
| dc.type | Article |











