Novel bis(thiosemicarbazones) of the 3,5-diacetyl-1,2,4-triazol series and their platinum(II) complexes: chemistry, antiproliferative activity and preliminary nephrotoxicity studies

被引:42
作者
Matesanz, Ana I. [1 ]
Hernandez, Carolina [1 ,2 ]
Rodriguez, Ana [3 ]
Souza, Pilar [1 ]
机构
[1] Univ Autonoma Madrid, Fac Ciencias, Dept Quim Inorgan Modulo 07, E-28049 Madrid, Spain
[2] Univ Castilla La Mancha, Fac Ciencias Medio Ambiente, Dept Quim Inorgan Organ & Bioquim, Toledo 45071, Spain
[3] Univ Castilla La Mancha, ETS Ingenieros Ind, Dept Quim Inorgan Organ & Bioquim, E-13071 Ciudad Real, Spain
关键词
TRIAPINE 3-AMINOPYRIDINE-2-CARBOXALDEHYDE THIOSEMICARBAZONE; CRYSTAL-STRUCTURE; RIBONUCLEOTIDE REDUCTASE; CYTOTOXIC ACTIVITY; DNA-BINDING; 1,2,4-TRIAZOLE; PALLADIUM(II); APOPTOSIS; INHIBITOR; TOXICITY;
D O I
10.1039/c1dt10212e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The preparation and characterization of three novel N-4-monosubstituted bis(thiosemicarbazone) ligands of 3,5-diacetyl-1,2,4-triazol series and their dinuclear platinum complexes are described. The crystal and molecular structure of the [Pt(mu-H3L3)](2) complex derived of 3,5-diacetyl-1,2,4-triazol bis(N-4-p-tolylthiosemicarbazone), H5L3, has been resolved by single crystal X-ray diffraction. The ligands coordinate, in an asymmetric dideprotonate form, to the platinum ions in a tridentate fashion (NNS) and S-bridging bonding modes. Thus the molecular units of the platinum complexes are stacked as dimers. The new compounds synthesized have been evaluated for antiproliferative activity in vitro against NCI-H460, A2780 and A2780cisR human cancer cell lines. The cytotoxicity data suggest that these compounds may be endowed with important antitumour properties since are capable of not only circumventing cisplatin resistance in A2780cisR cells but also exhibit high antiproliferative activity in human non-small cell lung cancer NCI-H460 cells. The interactions of these compounds with calf thymus DNA was investigated by UV-vis absorption and a nephrotoxic study, in LLC-PK1 cells, has also been carried out.
引用
收藏
页码:5738 / 5745
页数:8
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