Synthesis, Characterization and Antiproliferative Activity of Transition Metal Complexes with 3-(4,5-Diphenyl-1,3-oxazol-2-yl)propanoic Acid (Oxaprozin)

被引:0
|
作者
Bozic, Bojan D. J. [1 ]
Rogan, Jelena R. [1 ]
Poleti, Dejan D. [1 ]
Trisovic, Nemanja P. [1 ]
Bozic, Biljana D. J. [2 ]
Uscumlic, Gordana S. [1 ]
机构
[1] Univ Belgrade, Fac Technol & Met, Belgrade 11000, Serbia
[2] Univ Belgrade, Fac Biol, Belgrade 11000, Serbia
关键词
oxaprozin; transition metal complex; antiferromagnetic interaction; cytotoxic effect; antiproliferative activity; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; ACTIVATED PROTEIN-KINASES; CYCLOOXYGENASE INHIBITORS; CARCINOMA-CELLS; APOPTOSIS; CANCER; INDUCTION; POTENT;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) complexes with oxaprozin (Hoxa), a nonsteroidal anti-inflammatory drug, has been synthesized. The drug and complexes have been characterized by elemental and thermogravimetric (TG) analysis, Fourier transform (FT)-IR, H-1-NMR, C-13-NMR, UV-Vis spectroscopy and magnetic susceptibility measurements. The (pseudo)octahedral geometry has been proposed for all complexes based on electronic spectra and magnetic moments. With exception of the Cu(II) complex, where bridging bidentate mode of COO groups has been found, FT-IR spectra confirmed chelately coordinated COO groups in the other complexes. The general formula of the complexes is [M(H2O)(2)(oxa)(2)]center dot xH(2)O, with x=2 for M=Mn, Co and Ni and x=1.5 for Zn. The binuclear Cu(II) complex, [Cu-2(H2O)(2)(OH)(oxa)(3)]center dot 2H(2)O, has strong Cu-Cu interactions of antiferromagnetic type. The complexes and Hoxa did not exhibit the cytotoxic effect to peritoneal macrophages. For the first time these complexes have been tested for their in vitro antiproliferative activity against human colon and breast cancer cell lines, HCT-116 and MDA-231, respectively. For all investigated compounds significant antiproliferative effects have been observed. Ni(II) complex has been shown to be a promising antiproliferative agent exerting excellent activity against HCT-116 even in nanomolar concentrations.
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收藏
页码:865 / 869
页数:5
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