Novel Zn(II), Co(II) and Cu(II) diflunisalato complexes with neocuproine and their exceptional antiproliferative activity against cancer cell lines
Three novel complexes of deprotonated diflunisal ( ) with neocuproine ( ) were synthesized and characterized elemental, spectral (UV-vis, FTIR, fluorescence, and mass spectrometry), and single-crystal X-ray diffraction analyses. Although the compounds shared a similar composition of [MCl( )( )], whe...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2024-11, Vol.53 (43), p.17595-17607 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Three novel complexes of deprotonated diflunisal (
) with neocuproine (
) were synthesized and characterized
elemental, spectral (UV-vis, FTIR, fluorescence, and mass spectrometry), and single-crystal X-ray diffraction analyses. Although the compounds shared a similar composition of [MCl(
)(
)], where M represents Zn(II) (1), Co(II) (2) and Cu(II) (3), only 1 and 2 were isostructural, while 3 differed in both the molecular and supramolecular structures. In all three complex molecules, the central atom is coordinated by two nitrogen atoms of
in a bidentate chelate mode, and one chlorido ligand and
is bonded in either a monodentate mode
one oxygen atom of the carboxylate in 1 and 2 or in a bidentate chelate mode
both carboxylate oxygen atoms in 3. All three compounds demonstrated remarkable antiproliferative activity against human prostate (PC-3), colon (HCT116) and breast (MDA-MB-468) cancer cell lines with IC
values in the nanomolar range, with the lowest values observed in the case of PC-3 and MDA-MB-468 with 2 (20.0 nM) and 3 (31.1 nM), respectively. Moreover, complex 2, as the most active, was further investigated for its potential to induce perturbations in the cell cycle of PC-3 cells. The results indicated an induction of caspase-independent apoptosis. The interaction of the complexes with genomic DNA isolated from the respective cancer cell lines was evaluated for the intercalative mode, with binding strength correlated with the antiproliferative activity against PC-3 and MDA-MB-468 cancer cell lines. |
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ISSN: | 1477-9226 1477-9234 1477-9234 |
DOI: | 10.1039/d4dt01736f |