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Synthesis, characterization, in vitro antitumor activity, DNA-binding properties and electronic structure (DFT) of the new complex cis-(Cl,Cl)[RuIICl2(NO+)(terpy)]Cl
- Source :
- Dalton Transactions. :1176
- Publication Year :
- 2005
- Publisher :
- Royal Society of Chemistry (RSC), 2005.
-
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 µM. 31P and 23Na NMR spectroscopy along with electrophoretic mobility studies illustrated that complex 1 primarily binds by coordination to DNA without any π-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.
- Subjects :
- Spectrometry, Mass, Electrospray Ionization
Magnetic Resonance Spectroscopy
Stereochemistry
Guanine
Ligand
Antineoplastic Agents
Electrophoretic Mobility Shift Assay
DNA
Electronic structure
Nucleic Acid Denaturation
Nucleobase
Inorganic Chemistry
chemistry.chemical_compound
chemistry
Cell Line, Tumor
Humans
Ruthenium Compounds
Terpyridine
Acetonitrile
Cytosine
Subjects
Details
- ISSN :
- 14779234 and 14779226
- Database :
- OpenAIRE
- Journal :
- Dalton Transactions
- Accession number :
- edsair.doi.dedup.....b2a30cba9e85425698ac5fed1054c913