Investigating the anticancer potential of 4-phenylthiazole derived Ru(ii) and Os(ii) metalacycles

In this contribution we report the synthesis, characterization and in vitro anticancer activity of novel cyclometalated 4-phenylthiazole-derived ruthenium(ii) (2a-e) and osmium(ii) (3a-e) complexes. Formation and sufficient purity of the complexes were unambigiously confirmed by H-1-, C-13- and 2D-N...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Getreuer Paul
Marretta Laura
Toyoglu Emine
Dömötör Orsolya
Hejl Michaela
Prado-Roller Alexander
Cseh Klaudia
Legin Anton A.
Jakupec Michael A.
Barone Giampaolo
Terenzi Alessio
Keppler Bernhard K.
Kandioller Wolfgang
Dokumentumtípus: Cikk
Megjelent: 2024
Sorozat:DALTON TRANSACTIONS 53 No. 12
Tárgyszavak:
doi:10.1039/d4dt00245h

mtmt:34773647
Online Access:http://publicatio.bibl.u-szeged.hu/32371
Leíró adatok
Tartalmi kivonat:In this contribution we report the synthesis, characterization and in vitro anticancer activity of novel cyclometalated 4-phenylthiazole-derived ruthenium(ii) (2a-e) and osmium(ii) (3a-e) complexes. Formation and sufficient purity of the complexes were unambigiously confirmed by H-1-, C-13- and 2D-NMR techniques, X-ray diffractometry, HRMS and elemental analysis. The binding preferences of these cyclometalates to selected amino acids and to DNA models including G-quadruplex structures were analyzed. Additionally, their stability and behaviour in aqueous solutions was determined by UV-Vis spectroscopy. Their cellular accumulation, their ability of inducing apoptosis, as well as their interference in the cell cycle were studied in SW480 colon cancer cells. The anticancer potencies were investigated in three human cancer cell lines and revealed IC50 values in the low micromolar range, in contrast to the biologically inactive ligands.
Terjedelem/Fizikai jellemzők:5567-5579
ISSN:1477-9226