3-Hydroxyflavones vs. 3-hydroxyquinolinones: Structure-activity relationships and stability studies on RuII(arene) anticancer complexes with biologically active ligands

Andrea Kurzwernhart, Wolfgang Kandioller, Éva A. Enyedy, Maria Novak, Michael A. Jakupec, Bernhard K. Keppler, Christian G. Hartinger

Research output: Contribution to journalArticle

65 Citations (Scopus)


RuII6-arene) complexes, especially with bioactive ligands, are considered to be very promising compounds for anticancer drug design. We have shown recently that RuII6-p- cymene) complexes with 3-hydroxyflavone ligands exhibit very high in vitro cytotoxic activities correlating with a strong inhibition of topoisomerase IIα. In order to expand our knowledge about the structure-activity relationships and to determine the impact of lipophilicity of the arene ligand and of the hydrolysis rate on anticancer activity, a series of novel 3-hydroxyflavone derived RuII6-arene) complexes were synthesised. Furthermore, the impact of the heteroatom in the bioactive ligand backbone was studied by comparing the cytotoxic activity of Ru II6-p-cymene) complexes of 3-hydroxyquinolinone ligands with that of their 3-hydroxyflavone analogues. To better understand the behaviour of these RuII complexes in aqueous solution, the stability constants and pKa values for complexes and the corresponding ligands were determined. Furthermore, the interaction with the DNA model 5′-GMP and with a series of amino acids was studied in order to identify potential biological target structures.

Original languageEnglish
Pages (from-to)6193-6202
Number of pages10
JournalDalton Transactions
Issue number17
Publication statusPublished - May 7 2013

ASJC Scopus subject areas

  • Inorganic Chemistry

Fingerprint Dive into the research topics of '3-Hydroxyflavones vs. 3-hydroxyquinolinones: Structure-activity relationships and stability studies on Ru<sup>II</sup>(arene) anticancer complexes with biologically active ligands'. Together they form a unique fingerprint.

  • Cite this