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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Karidi, K. | en |
| dc.contributor.author | Garoufis, A. | en |
| dc.contributor.author | Tsipis, A. | en |
| dc.contributor.author | Hadjiliadis, N. | en |
| dc.contributor.author | den Dulk, H. | en |
| dc.contributor.author | Reedijk, J. | en |
| dc.date.accessioned | 2015-11-24T16:49:33Z | - |
| dc.date.available | 2015-11-24T16:49:33Z | - |
| dc.identifier.issn | 1477-9226 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9501 | - |
| dc.rights | Default Licence | - |
| dc.subject | density-functional-theory | en |
| dc.subject | ruthenium polypyridine complexes | en |
| dc.subject | effective core potentials | en |
| dc.subject | metal nitrosyl complexes | en |
| dc.subject | nitric-oxide release | en |
| dc.subject | x-ray-structure | en |
| dc.subject | molecular-structure | en |
| dc.subject | infrared-spectra | en |
| dc.subject | aqueous-solution | en |
| dc.subject | linkage isomers | en |
| dc.title | Synthesis, characterization, in vitro antitumor activity, DNA-binding properties and electronic structure (DFT) of the new complex cis-(Cl,Cl)[Ru(II)Cl2(NO+)(terpy)]Cl | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | Doi 10.1039/B418838a | - |
| heal.identifier.secondary | <Go to ISI>://000227792200006 | - |
| heal.identifier.secondary | http://pubs.rsc.org/en/content/articlepdf/2005/dt/b418838a | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.publicationDate | 2005 | - |
| heal.abstract | The complex cis-(Cl,Cl)-[RuCl2(terpy)( NO)]Cl(1) has been synthesized by the reaction of [RuCl3(H2O)(2)(NO)] with terpyridine (terpy) and characterized by various spectroscopic, analytical techniques and using electronic structure calculation (DFT) methods. The cytotoxic activity and the DNA-binding properties of 1 have also been studied using biochemical techniques. The results establish unequivocally that 1 corresponds to a so-called [RuNO](6) species, which readily releases the nitrosyl ligand upon irradiation with a mercury lamp in acetonitrile solution. DFT calculations provided a satisfactory description of structural, bonding, electronic and related properties of the new compound and throw light on the mechanism of the photo-induced NO release. Screening on A2780 (human ovarian carcinoma) cell lines showed significant cytotoxicity with an IC50 value of 0.49 mu M. P-31 and Na-23 NMR spectroscopy along with electrophoretic mobility studies illustrated that complex 1 primarily binds by coordination to DNA without any pi-interaction between the planar terpy ligand and the DNA bases, while weak electrostatic interactions could not be excluded. Studies on the inhibition of the restriction enzymes DraI and SmaI revealed that 1 prefers the guanine and cytosine bases of DNA. | en |
| heal.publisher | Royal Society of Chemistry | en |
| heal.journalName | Dalton Transactions | en |
| heal.journalType | peer reviewed | - |
| heal.fullTextAvailability | TRUE | - |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Karidi-2005-Synthesis, character.pdf | 474.92 kB | Adobe PDF | View/Open Request a copy |
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