DSpace@İnönü

Synthesis and investigation of antiproliferative activity of Ru-NHC complexes against C6 and HeLa cancer cells

Basit öğe kaydını göster

dc.contributor.author Paşahan, R.
dc.contributor.author Akkoç, M.
dc.contributor.author Yaşar, Ş.
dc.contributor.author Kul Köprülü, T.
dc.contributor.author Tekin, Ş.
dc.contributor.author Yaşar, S.
dc.contributor.author Özdemir, İ.
dc.date.accessioned 2022-10-06T12:54:41Z
dc.date.available 2022-10-06T12:54:41Z
dc.date.issued 2022
dc.identifier.issn 13000527 (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/72391
dc.description.abstract The 2-methylpyridine, 2-diethylaminoethyl, and isopentyl linked a series of symmetric and unsymmetric benzimidazolium salts 2a-e were prepared and used in the synthesis of silver-N-heterocyclic carbene (NHC) complexes (3a-e). The Ru(II)-NHC complexes (4a-h) were synthesized via transmetalation reaction from 3a-e. 4a-h complexes were converted to Ru(II)-NHC.HCl complexes (5a-h) by HCl solution of diethyl ether and characterized by different spectroscopic techniques such as 1H and 13C NMR, LC/MS-Q-TOF, FT-IR, elemental analysis, and melting point detection. We examined the effect of the structural difference of complexes on anticancer activity via different arenes and metal centers. Antiproliferative activity of 5a-h and 3a was tested against human cervix adenocarcinoma (HeLa) and rat glioblastoma (C6) cell lines by ELISA assay. The IC50 value of 5b, 5c and 5e complexes exhibited good cytotoxic activity than cisplatin on C6 (14.2 ± 0.5 mM; 16.2 ± 0.4 mM; 24.2 ± 0.7 mM, respectively) and HeLa (11.1 ± 0.5 mM; 13.7 ± 0.3 mM; 22.8 ± 0.8 mM, respectively) cell lines. © 2022 TUBITAK. All rights reserved.
dc.source Turkish Journal of Chemistry
dc.title Synthesis and investigation of antiproliferative activity of Ru-NHC complexes against C6 and HeLa cancer cells


Bu öğenin dosyaları:

Dosyalar Boyut Biçim Göster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster