http://www.cnr.it/ontology/cnr/individuo/prodotto/ID170080
Amphiphilic N-glycosyl-thiocarbamoyl cyclodextrins: synthesis, self-assembly, and fluorimetry of recognition by Lens culinaris lectin (Articolo in rivista)
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- Label
- Amphiphilic N-glycosyl-thiocarbamoyl cyclodextrins: synthesis, self-assembly, and fluorimetry of recognition by Lens culinaris lectin (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/bm070055u (literal)
- Alternative label
S. McNicholas; A. Rencurosi; L. Lay; A. Mazzaglia; L. Sturiale; M. Perez; R. Darcy (2007)
Amphiphilic N-glycosyl-thiocarbamoyl cyclodextrins: synthesis, self-assembly, and fluorimetry of recognition by Lens culinaris lectin
in Biomacromolecules; ACS, American chemical society, Washington, DC (Stati Uniti d'America)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- S. McNicholas; A. Rencurosi; L. Lay; A. Mazzaglia; L. Sturiale; M. Perez; R. Darcy (literal)
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- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
- No. Citazione=2;
Autocitazione=2;
Motore utilizzato per le citazioni=Isiwebofknowledge.com (literal)
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- Scopu (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Centre for Synthesis and Chemical Biology of the Conway Institute, School of Chemistry and Chemical
Biology, University College Dublin, Belfield, Dublin 4, Ireland, Dipartimento di Chimica Organica e
Industriale, Universita` di Milano, Via Venezian 21, 20133 Milano, Italy, Istituto per lo Studio dei Materiali
Nanostrutturati, Consiglio Nazionale delle Ricerche, Salita Sperone 31, 98166 Messina, Italy, and Istituto di
Chimica e Tecnologia dei Polimeri, Consiglio Nazionale delle Ricerche, Viale R. Margherita 6,
95123 Catania, Italy (literal)
- Titolo
- Amphiphilic N-glycosyl-thiocarbamoyl cyclodextrins: synthesis, self-assembly, and fluorimetry of recognition by Lens culinaris lectin (literal)
- Abstract
- Amphiphilic beta-cyclodextrins have been synthesized bearing hexylthio, dodecylthio, and hexadecylthio chains at the 6-positions and glycosylthiocarbamoyl-oligo(ethylene glycol) units at the 2-positions. The glycosyl residues (±-D-mannosyl and ²-L-fucosyl) are intended for cell-targeting. Self-assembly of these new amphiphilic glycosylated cyclodextrins in water to form vesicles was investigated by dynamic light scattering and transmission electron microscopy. Selective binding of the hexylthio assemblies to a protein receptor (Lens culinaris lectin) was confirmed by fluorescence spectroscopy. (literal)
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