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  4. Antiproliferative activity of chelating N,O- and N,N-ruthenium(II) arene functionalised poly(propyleneimine) dendrimer scaffolds
 
research article

Antiproliferative activity of chelating N,O- and N,N-ruthenium(II) arene functionalised poly(propyleneimine) dendrimer scaffolds

Govender, P.
•
Renfrew, A. K.  
•
Clavel, C. M.  
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2011
Dalton Transactions

Chelating neutral (N,O) and cationic (N,N) first-and second-generation ruthenium(II) arene metallodendrimers based on poly(propyleneimine) dendrimer scaffolds were obtained from dinuclear arene ruthenium precursors by reactions with salicylaldimine and iminopyridyl dendritic ligands, respectively. The N, N cationic complexes were isolated as hexafluorophosphate salts and were characterised by NMR and IR spectroscopy, and MALDI-TOF mass spectrometry. Related mononuclear complexes were obtained in a similar manner and their molecular structures have been determined by X-ray diffraction analysis. The cytotoxicities of the mono-and multinuclear complexes were established using A2780 and A2780cisR human ovarian carcinoma cancer cell lines.

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Type
research article
DOI
10.1039/c0dt00761g
Web of Science ID

WOS:000286390300023

Author(s)
Govender, P.
Renfrew, A. K.  
Clavel, C. M.  
Dyson, P. J.  
Therrien, B.
Smith, G. S.
Date Issued

2011

Published in
Dalton Transactions
Volume

40

Article Number

1158

Subjects

Ruthenium Complexes

•

Anticancer Activity

•

Molecular-Structure

•

Metal-Complexes

•

In-Vitro

•

Antitumor-Activity

•

Catalytic-Activity

•

Ruthenium(Ii)-Arene Complexes

•

Preclinical Development

•

Nickel-Catalysts

Editorial or Peer reviewed

NON-REVIEWED

Written at

EPFL

EPFL units
LCOM  
Available on Infoscience
March 9, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/65223
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