MersV1, Main, Exploration, bibRecord, 003557

Fullerene‐based amino acids and peptides

Identifieur interne : 003557 ( Main/Exploration ); précédent : 003556; suivant : 003558

Fullerene‐based amino acids and peptides

Auteurs : Alberto Bianco [France] ; Tatiana Da Ros [Italie] ; Maurizio Prato [Italie] ; Claudio Toniolo [Italie]

Source :

Journal of Peptide Science [ 1075-2617 ] ; 2001-04.

RBID : ISTEX:9596911AA34D992AB58BA0CBF7D3FBCB45606A93

English descriptors

Teeft :
- Acid, Acid derivatives, Agents chemother, Amino, Amino acid, Amino acid derivatives, Amino acids, Azomethine ylides, Bacterial meningitis, Bianco, Biological activity, Biological applications, Biological properties, Carboxylic, Carboxylic acid, Carboxylic function, Cerebellar granule cells, Chem, Chlorinated solvents, Coli growth, Commun, Conformational characterization, Copyright, Derivative, European peptide society, Exchange interaction, Febs lett, Fullerene, Fullerene derivatives, Fullerene moiety, Fullerene spheroid, Fulleroamino, Fulleroamino acid, Fulleroamino acids, Fulleroproline, Fulleroproline derivatives, Interesting activity, Intramolecular electron transfer, John wiley sons, Laurea degree, Lett, Lipid peroxidation, Maggini, Many classes, Materials science, Medicinal chemistry, Methanofullerene carboxylic acid, Moiety, Mouse embryos, Neuroprotective agents, Novel derivatives, Novel fullerene derivatives, Organic chemistry, Padova, Peptide, Peptide synthesis, Pharmaceutical chemistry, Prato, Racemic mixture, Scorrano, Side chain, Stationary phase, Stereoselective synthesis, Structural studies, Tertiary amide bond, Tetrahedron lett, Toluene solution, Toniolo, Trans equilibrium, Wudl.

Abstract

Recent advances in the chemistry of fullerene have allowed the synthesis of many classes of novel fullerene derivatives. Among these classes, fullerene‐based amino acids and peptides are particularly interesting, both for structural studies and biological applications. In this review, we will discuss our own achievements in this rapidly growing field. In particular, the application of fulleroproline (Fpr) amino acids and peptides to medicinal chemistry and material science will be highlighted. Copyright © 2001 European Peptide Society and John Wiley & Sons, Ltd.

Url:

https://api.istex.fr/ark:/67375/WNG-QSQD258K-8/fulltext.pdf

DOI: 10.1002/psc.313

Affiliations:

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Le document en format XML

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<author><name sortKey="Prato, Maurizio" sort="Prato, Maurizio" uniqKey="Prato M" first="Maurizio" last="Prato">Maurizio Prato</name>
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<term>Amino acid derivatives</term>
<term>Amino acids</term>
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<term>Bacterial meningitis</term>
<term>Bianco</term>
<term>Biological activity</term>
<term>Biological applications</term>
<term>Biological properties</term>
<term>Carboxylic</term>
<term>Carboxylic acid</term>
<term>Carboxylic function</term>
<term>Cerebellar granule cells</term>
<term>Chem</term>
<term>Chlorinated solvents</term>
<term>Coli growth</term>
<term>Commun</term>
<term>Conformational characterization</term>
<term>Copyright</term>
<term>Derivative</term>
<term>European peptide society</term>
<term>Exchange interaction</term>
<term>Febs lett</term>
<term>Fullerene</term>
<term>Fullerene derivatives</term>
<term>Fullerene moiety</term>
<term>Fullerene spheroid</term>
<term>Fulleroamino</term>
<term>Fulleroamino acid</term>
<term>Fulleroamino acids</term>
<term>Fulleroproline</term>
<term>Fulleroproline derivatives</term>
<term>Interesting activity</term>
<term>Intramolecular electron transfer</term>
<term>John wiley sons</term>
<term>Laurea degree</term>
<term>Lett</term>
<term>Lipid peroxidation</term>
<term>Maggini</term>
<term>Many classes</term>
<term>Materials science</term>
<term>Medicinal chemistry</term>
<term>Methanofullerene carboxylic acid</term>
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<term>Mouse embryos</term>
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<term>Prato</term>
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<term>Scorrano</term>
<term>Side chain</term>
<term>Stationary phase</term>
<term>Stereoselective synthesis</term>
<term>Structural studies</term>
<term>Tertiary amide bond</term>
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<front><div type="abstract" xml:lang="en">Recent advances in the chemistry of fullerene have allowed the synthesis of many classes of novel fullerene derivatives. Among these classes, fullerene‐based amino acids and peptides are particularly interesting, both for structural studies and biological applications. In this review, we will discuss our own achievements in this rapidly growing field. In particular, the application of fulleroproline (Fpr) amino acids and peptides to medicinal chemistry and material science will be highlighted. Copyright © 2001 European Peptide Society and John Wiley & Sons, Ltd.</div>
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Fullerene‐based amino acids and peptides

Fullerene‐based amino acids and peptides

Source :

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri