In:
European Journal of Inorganic Chemistry, Wiley, Vol. 2018, No. 20-21 ( 2018-06-07), p. 2461-2470
Kurzfassung:
We report the synthesis, characterization, and biological activity of Ir I complexes with triazole‐ (NNHC) and thiazole‐based (NSHC) N‐heterocyclic carbene ligands. Starting from the dimeric [Ir(COD)Cl] 2 , we obtained complexes of composition Ir(COD)(NNHC)Cl ( 4a ), Ir(COD)(NNHC)X ( 4b : X = Cl; 4bBr : X = Br), [Ir(COD)(NNHC)(NHC)]I ( 5a ), [Ir(COD)(NSHC) 2 ]Cl ( 6a ), and [Ir(COD)(NSHC)(NNHC)]Cl ( 6b ) by adaptation of established synthetic methods for metal–NHC complexes. Their interactions with model proteins cytochrome c and lysozyme, as well as with the oligonucleotide hexamer (CG) 3 (ODN1), were studied. Although most complexes did not show any strong interactions with these biomolecules, all complexes were active against HT‐29 and MCF‐7 cancerous cells, with IC 50 values ranging between 1 and 60 µ m . The most active compounds were the cationic bis(carbene) derivatives 5 and 6 . All compounds generated high levels of reactive oxygen species (ROS) after incubation for 48 h in MCF‐7 cells, possibly suggesting a redox‐mediated mechanism of action. Interestingly, there were distinctive differences in the superoxide/(total ROS) ratios induced by the different groups of compounds.
Materialart:
Online-Ressource
ISSN:
1434-1948
,
1099-0682
DOI:
10.1002/ejic.v2018.20-21
DOI:
10.1002/ejic.201800225
Sprache:
Englisch
Verlag:
Wiley
Publikationsdatum:
2018
ZDB Id:
1475009-0
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