http://www.cnr.it/ontology/cnr/individuo/prodotto/ID14149
Synthesis of a novel Fmoc-protected nucleoaminoacid for the solid phase assembly of 4-piperidyl glycine/L-arginine-containing nucleopeptides and preliminary RNA interaction studies (Articolo in rivista)
- Type
- Label
- Synthesis of a novel Fmoc-protected nucleoaminoacid for the solid phase assembly of 4-piperidyl glycine/L-arginine-containing nucleopeptides and preliminary RNA interaction studies (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1007/s00726-010-0532-4 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Roviello GN; Crescenzo C; Capasso D.; Di Gaetano S.; Franco S; Bucci EM; Pedone C (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- Scopu (literal)
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- G. N. Roviello (&) ? C. Crescenzo ? S. Di Gaetano ?
S. Franco ? E. M. Bucci
Istituto di Biostrutture e Bioimmagini, CNR,
Via Mezzocannone 16, 80134 Naples, Italy
e-mail: giroviel@unina.it
D. Capasso ? C. Pedone
Dipartimento delle Scienze Biologiche, Universita` di Napoli
''Federico II'', 80134 Naples, Italy (literal)
- Titolo
- Synthesis of a novel Fmoc-protected nucleoaminoacid for the solid phase assembly of 4-piperidyl glycine/L-arginine-containing nucleopeptides and preliminary RNA interaction studies (literal)
- Abstract
- In this work, we report the synthesis of a novel
Fmoc-protected nucleoaminoacid, based on 4-piperidinyl
glycine, carrying the DNA nucleobase on the secondary
amino group, suitable for the solid-phase synthesis of nucleopeptides.
After ESI-MS and NMR characterization this
building block was used for the assembly of a thyminefunctionalized
tetrapeptide, composed of 4-piperidinyl
glycine and L-arginine moieties alternated in the backbone.
The ability to interact with RNA and the efficiency in
interfering with the reverse transcription of eukaryotic
mRNA of the novel nucleo-tetrapeptide found in this study
are in favour of the employment of chiral nucleopeptides
based on alternate 4-piperidinyl glycine/L-arginine backbone
in biomedicine. (literal)
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