Synthesis, Antiproliferative Activity and In Silico Studies of Chalcones Derived From 4-(Imidazole-1-yl)Acetophenone
| dc.contributor.author | AKTAR, BEDRİYE SEDA KURSUN | |
| dc.contributor.author | AL-KARABASH, ABDULRAHEEM MUSTAFA IBRAHIM | |
| dc.contributor.author | Yaglioglu, Ayse Sahin | |
| dc.contributor.author | oruç-emre, emine elçin | |
| dc.date.accessioned | 2025-10-24T18:03:36Z | |
| dc.date.available | 2025-10-24T18:03:36Z | |
| dc.date.issued | 2023 | |
| dc.department | Malatya Turgut Özal Üniversitesi | |
| dc.description.abstract | In this study, the synthesis of chalcone compounds (1-11) derived from 4-(imidazol-1-yl)acetophenone and the structure determination of these compounds by various spectroscopic methods were carried out. The anticancer activities of compounds 1-11 were examined against HeLa and PC-3 cancer cells at four different concentrations (100, 50, 25, and 5 µM) using the BrdU ELISA assay. It was determined that all molecules except compounds 1 and 6 in HeLa cancer cells and compounds 2 and 8 against PC-3 cancer cells were more active against HeLa and PC-3 than the standard drug 5-fluorouracil (5-FU). The best activity against PC-3 cancer cells was compound 4 (IC50: 1.39±0.00 µM). In addition, compound 11 (IC50: 1.58±0.01 µM) was found to have the highest activity against HeLa cancer cells. Compound 4 against PC-3 cancer cell and compound 11 against HeLa cancer cell displayed cell selective activity. The ADME properties and drug similarities of the molecules 1-11 using the SwissADME software were investigated. According to these properties, compounds 1-11 were found to obey Lipinski rules. | |
| dc.identifier.doi | 10.18596/jotcsa.1313595 | |
| dc.identifier.endpage | 868 | |
| dc.identifier.issn | 2149-0120 | |
| dc.identifier.issue | 3 | |
| dc.identifier.startpage | 861 | |
| dc.identifier.trdizinid | 1195528 | |
| dc.identifier.uri | https://doi.org/10.18596/jotcsa.1313595 | |
| dc.identifier.uri | https://search.trdizin.gov.tr/tr/yayin/detay/1195528 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12899/2324 | |
| dc.identifier.volume | 10 | |
| dc.indekslendigikaynak | TR-Dizin | |
| dc.language.iso | en | |
| dc.relation.ispartof | Journal of the Turkish Chemical Society, Section A: Chemistry | |
| dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | TR-Dizin_20251023 | |
| dc.subject | Kimya | |
| dc.subject | Tıbbi | |
| dc.subject | Biyoteknoloji ve Uygulamalı Mikrobiyoloji | |
| dc.subject | Onkoloji | |
| dc.subject | ADME | |
| dc.subject | antiproliferative activity | |
| dc.subject | HeLa cell line | |
| dc.subject | in silico. | |
| dc.subject | PC-3 cell line | |
| dc.title | Synthesis, Antiproliferative Activity and In Silico Studies of Chalcones Derived From 4-(Imidazole-1-yl)Acetophenone | |
| dc.type | Article |












