Organometallic Ruthenium and Osmium Compounds of Pyridin-2-and-4-ones as Potential Anticancer Agents

被引:15
作者
Henke, Helena [1 ,2 ]
Kandioller, Wolfgang [1 ]
Hanif, Muhammad [3 ]
Keppler, Bernhard K. [1 ,2 ]
Hartinger, Christian G. [1 ,2 ,4 ]
机构
[1] Univ Vienna, Inst Inorgan Chem, AT-1090 Vienna, Austria
[2] Univ Vienna, AT-1090 Vienna, Austria
[3] COMSATS Inst Informat Technol, Dept Chem, Abbottabad 22060, Pakistan
[4] Univ Auckland, Sch Chem Sci, Auckland 1010, New Zealand
基金
奥地利科学基金会;
关键词
Bioorganometallics; Anticancer activity; Ruthenium complexes; Pyridinones; Osmium complexes; MRI CONTRAST AGENTS; IN-VITRO; IRON(III)-CHELATING PROPERTIES; METAL-COMPOUNDS; COMPLEXES; LIGANDS; INHIBITORS; CHEMISTRY; MALTOL; DRUGS;
D O I
10.1002/cbdv.201200005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Organometallic RuII compounds are among the most widely studied anticancer agents. Functionalizing metal centers with biomolecule-derived ligands has been shown to be a promising strategy to improve the antiproliferative activity of metal-based chemotherapeutics. Herein, the synthesis of a series of novel 3-hydroxypyridin-2-one-derived ligands and their MII(?6-p-cymene) half-sandwich complexes (M=Ru, Os) is described. The compounds were characterized by 1D- and 2D-NMR spectroscopy, and elemental analysis.
引用
收藏
页码:1718 / 1727
页数:10
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