Synthesis and Analysis of the Structure, Diffusion and Cytotoxicity of Heterocyclic Platinum(IV) Complexes

被引:30
|
作者
Macias, Freddy J. [1 ]
Deo, Krishant M. [1 ]
Pages, Benjamin J. [1 ]
Wormell, Paul [1 ]
Clegg, Jack K. [2 ]
Zhang, Yingjie [3 ]
Li, Feng [1 ]
Zheng, Gang [1 ]
Sakoff, Jennette [4 ]
Gilbert, Jayne [4 ]
Aldrich-Wright, Janice R. [1 ]
机构
[1] Univ Western Sydney, Nanoscale Org & Dynam Grp, Campbelltown, NSW 2560, Australia
[2] Univ Queensland, Sch Chem & Mol Biosci, St Lucia, Qld 4072, Australia
[3] Australian Nucl Sci & Technol Org, Kirrawee Dc, NSW 2232, Australia
[4] Calvary Mater Newcastle, Waratah, NSW 2298, Australia
关键词
antitumor agents; cancer; cytotoxicity; platinum; X-ray diffraction; ELECTROCHEMICAL REDUCTION; LUMINESCENCE PROPERTIES; ANTICANCER ACTIVITY; NMR-SPECTROSCOPY; PT-IV; MECHANISMS; METALLOINTERCALATORS; AGGREGATION; ABSORPTION; STACKING;
D O I
10.1002/chem.201502159
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed six dihydroxidoplatinum(IV) compounds with cytotoxic potential. Each derived from active platinum(II) species, these complexes consist of a heterocyclic ligand (H-L) and ancillary ligand (A(L)) in the form [Pt(H-L)(A(L))(OH)(2)](2+), where H-L is a methyl-functionalised variant of 1,10-phenanthroline and A(L) is the S,S or R,R isomer of 1,2-diaminocyclohexane. NMR characterisation and X-ray diffraction studies clearly confirmed the coordination geometry of the octahedral platinum(IV) complexes. The self-stacking of these complexes was determined using pulsed gradient stimulated echo nuclear magnetic resonance. The self-association behaviour of square planar platinum(II) complexes is largely dependent on concentration, whereas platinum(IV) complexes do not aggregate under the same conditions, possibly due to the presence of axial ligands. The cytotoxicity of the most active complex, exhibited in several cell lines, has been retained in the platinum(IV) form.
引用
收藏
页码:16990 / 17001
页数:12
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