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Transition Metal Complexes with 1‐Adamantoyl Hydrazones – Cytotoxic Copper(II) Complexes of Tri‐ and Tetradentate Pyridine Chelators Containing an Adamantane Ring System
Author(s) -
Leovac Vukadin M.,
Rodić Marko V.,
Jovanović Ljiljana S.,
Joksović Milan D.,
Stanojković Tatjana,
Vujčić Miroslava,
Sladić Dušan,
Marković Violeta,
VojinovićJešić Ljiljana S.
Publication year - 2015
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201403050
Subject(s) - chemistry , copper , crystallography , hydrazone , pyridine , stereochemistry , fluorescence , metal , medicinal chemistry , organic chemistry , physics , quantum mechanics
Five pentacoordinate copper(II) complexes with 2‐acetylpyridine or di(2‐pyridyl) ketone 1‐adamantoyl hydrazone ligands (Adpy and Addpy, respectively) of the formulae [CuCl 2 (Adpy)] ( 1 ), [Cu 2 (μ‐Cl) 2 (Adpy‐H) 2 ] ( 2 ), [Cu(NCS) 2 (Adpy)] ( 3 ), [Cu 2 (μ‐Cl) 2 (Addpy‐H) 2 ] ( 4 ), and [Cu 2 (NCS) 2 (μ‐Addpy‐H) 2 ] ( 5 ) were synthesized and characterized by spectral, electrochemical, and X‐ray structural analysis. Flow cytometry and morphological analysis confirmed that the copper(II) complexes 2 and 5 induced accumulation of a sub‐G1 phase population, and fluorescence microscopy indicated the presence of large cells in apoptosis. The interaction of the copper(II) complexes with calf thymus DNA (CT‐DNA) was monitored by changes in their UV/Vis spectra. The observed intrinsic binding constants for 2 and 5 ( K b = 1.77 × 10 6 and 3.58 × 10 6 M –1 , respectively) together with ethidium displacement fluorescence experiments indicate intercalative binding. Complexes 2 and 5 showed nuclease activity against pUC19 plasmid DNA.