| dc.creator |
Özçelik, Azime Berna |
|
| dc.creator |
Oruç, Hatice |
|
| dc.creator |
Akdağ, Mevlüt |
|
| dc.creator |
Arslan, Gülnur |
|
| dc.date |
2023-05-06T00:00:00Z |
|
| dc.date.accessioned |
2024-08-26T12:08:03Z |
|
| dc.date.available |
2024-08-26T12:08:03Z |
|
| dc.identifier |
0d606dce-4f66-4e85-b00c-e3bd47cc0080 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/0d606dce-4f66-4e85-b00c-e3bd47cc0080/oai |
|
| dc.identifier.uri |
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/98719 |
|
| dc.description |
<p>Breast cancer is the most common cause of cancer cases among women worldwide estimated to cause 1 million deaths in 2040 [1]. Heterocycles are important building blocks of anticancer agents [2]. Of the aromatic heterocycle compounds, it has been widely reported that nitrogenbased heterocycles and benzothiazole derivatives have anticancer properties [2-4]. In this study, benzothiazol-2(3H)-one and [1,2,4]triazolo[4,3-b]pyridazine cores were merged and 5-chloro-3-((6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)benzo[d]thiazol-2(3H)-one compound was designed. The compound was synthesized by both conventional and microwave irradiation methods. It was evaluated against MCF-7 breast cancer cells<br></p> |
|
| dc.language |
eng |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
SYNTHESIS AND ANTICANCER ACTIVITY OF 5- CHLORO-3-((6-CHLORO- [1,2,4]TRIAZOLO[4,3- b]PYRIDAZIN-3-YL)METHYL)BENZO[d]THIAZOL- 2(3H)- ONE |
|
| dc.type |
info:eu-repo/semantics/conferenceObject |
|