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research article

Synthesis and Biological Evaluation of Modified 2-Deoxystreptamine Dimers

Coste, Gerald
•
Horlacher, Tim
•
Molina, Lidia
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2011
Synthesis-Stuttgart

Aminoglycosides are powerful antibiotics, but the emergence of resistant bacterial strains has prompted the search for analogues with better pharmacological profiles. The synthesis of 2-deoxystreptamine (2-DOS) dimers linked by polyamines and analogues based on furylcarbopeptoid skeletons is described. Potent and selective ligands for bacterial 16S rRNA were identified using microarray techniques by determining the affinity of these derivatives toward bacterial and human ribosomal RNAs.

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Type
research article
DOI
10.1055/s-0030-1260033
Web of Science ID

WOS:000290787100014

Author(s)
Coste, Gerald
Horlacher, Tim
Molina, Lidia
Moreno-Vargas, Antonio J.
Carmona, Ana T.  
Robina, Inmaculada
Seeberger, Peter H.
Gerber-Lemaire, Sandrine  
Date Issued

2011

Published in
Synthesis-Stuttgart
Start page

1759

End page

1770

Subjects

antibiotics

•

2-deoxystreptamine dimers

•

microarray

•

ribosomal RNA

•

solid-phase synthesis

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSPN  
Available on Infoscience
June 17, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/68775
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