http://www.cnr.it/ontology/cnr/individuo/prodotto/ID195136
Aminopyrrolic Synthetic Receptors for Monosaccharides: A Class of Carbohydrate-Binding Agents Endowed with Antibiotic Activity vs. Pathogenic Yeasts (Articolo in rivista)
- Type
- Label
- Aminopyrrolic Synthetic Receptors for Monosaccharides: A Class of Carbohydrate-Binding Agents Endowed with Antibiotic Activity vs. Pathogenic Yeasts (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/chem.201103318 (literal)
- Alternative label
C. Nativi, O. Francesconi, G. Gabrielli, I. De Simone, B. Turchetti, T. Mello, L. Di Cesare Mannelli, C. Ghelardini, P. Buzzini, S. Roelens (2012)
Aminopyrrolic Synthetic Receptors for Monosaccharides: A Class of Carbohydrate-Binding Agents Endowed with Antibiotic Activity vs. Pathogenic Yeasts
in Chemistry - A European Journal
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- C. Nativi, O. Francesconi, G. Gabrielli, I. De Simone, B. Turchetti, T. Mello, L. Di Cesare Mannelli, C. Ghelardini, P. Buzzini, S. Roelens (literal)
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- Dipartimento di Chimica, Università di Firenze; Dipartimento di Biologia Applicata and Industrial Yeasts Collection DBVPG, Università di Perugia; Dipartimento di Fisiopatologia Clinica, Università di Firenze; Dipartimento di Farmacologia Preclinica e Clinica, Università di Firenze; Istituto di Metodologie Chimiche (IMC)
Consiglio Nazionale delle Ricerche (CNR). (literal)
- Titolo
- Aminopyrrolic Synthetic Receptors for Monosaccharides: A Class of Carbohydrate-Binding Agents Endowed with Antibiotic Activity vs. Pathogenic Yeasts (literal)
- Abstract
- The biological activity of a set of structurally related aminopyrrolic synthetic receptors for monosaccharides has been tested vs. yeast and yeast-like microorganisms and compared to their binding affinity toward mannosides. Antibiotic activity comparable to that of well-known polyene (amphotericin B) or azole (ketoconazole) drugs has been found for some members of the family, along with a general correlation with binding abilities. A systematic structure-activity-affinity investigation shed light on the structural and functional requirements necessary for antibiotic activity and identified the tripodal 1 as the most potent compound of the set. Together with toxicity tests and inhibitor localization experiments performed through fluorescence microscopy, these studies lead to the characterization of a new class of carbohydrate binding agents possessing antibiotic activity, in which pyrrolic groups precisely structured on a tripodal architecture appear to be responsible for permeability through the cell wall of pathogens, as well as for antibiotic activity inside the cytoplasm (literal)
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