کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1322831 | 1499908 | 2013 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Synthesis, characterization, electrochemical behavior and in vitro protein tyrosine kinase inhibitory activity of the cymene-halogenobenzohydroxamato [Ru(η6-cymene)(bha)Cl] complexes Synthesis, characterization, electrochemical behavior and in vitro protein tyrosine kinase inhibitory activity of the cymene-halogenobenzohydroxamato [Ru(η6-cymene)(bha)Cl] complexes](/preview/png/1322831.png)
The ruthenium(II)–cymene complexes [Ru(η6-cymene)(bha)Cl] with substituted halogenobenzohydroxamato (bha) ligands (substituents = 4-F, 4-Cl, 4-Br, 2,4-F2, 3,4-F2, 2,5-F2, 2,6-F2) have been synthesized and characterized by elemental analysis, IR, 1H NMR, 13C NMR, cyclic voltammetry and controlled-potential electrolysis, and density functional theory (DFT) studies. The compositions of their frontier molecular orbitals (MOs) were established by DFT calculations, and the oxidation and reduction potentials are shown to follow the orders of the estimated vertical ionization potential and electron affinity, respectively. The electrochemical EL Lever parameter is estimated for the first time for the various bha ligands, which can thus be ordered according to their electron-donor character. All complexes exhibit very strong protein tyrosine kinase (PTK) inhibitory activity, even much higher than that of genistein, the clinically used PTK inhibitory drug. The complex containing the 2,4-difluorobenzohydroxamato ligand is the most active one, and the dependences of the PTK activity of the complexes and of their redox potentials on the ring substituents are discussed.
The ruthenium(II)–cymene complexes [Ru(η6-cymene)(bha)Cl] with substituted halogenobenzohydroxamate (bha) ligands were synthesized and characterized. They exhibit very strong protein tyrosine kinase (PTK) inhibitory activity, much higher than that of genistein. The electrochemical EL Lever parameter is estimated for the bha ligands, which can thus be ordered according to their electron-donor character.Figure optionsDownload as PowerPoint slideHighlights
► Ru(II)–cymene complexes as powerful PTK inhibitors.
► Ru(II)–cymene complexes with PTK inhibitory activity higher than that of genistein.
► DFT calculations support electrochemical results.
► The Lever EL parameter for halogenobenzohydroxamate ligands is estimate.
Journal: Journal of Organometallic Chemistry - Volume 730, 15 April 2013, Pages 137–143