Fullerene‐based amino acids and peptides
Identifieur interne : 001B76 ( Istex/Corpus ); précédent : 001B75; suivant : 001B77Fullerene‐based amino acids and peptides
Auteurs : Alberto Bianco ; Tatiana Da Ros ; Maurizio Prato ; Claudio TonioloSource :
- Journal of Peptide Science [ 1075-2617 ] ; 2001-04.
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:
DOI: 10.1002/psc.313
Links to Exploration step
ISTEX:9596911AA34D992AB58BA0CBF7D3FBCB45606A93Le document en format XML
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science</term><term>Medicinal chemistry</term><term>Methanofullerene carboxylic acid</term><term>Moiety</term><term>Mouse embryos</term><term>Neuroprotective agents</term><term>Novel derivatives</term><term>Novel fullerene derivatives</term><term>Organic chemistry</term><term>Padova</term><term>Peptide</term><term>Peptide synthesis</term><term>Pharmaceutical chemistry</term><term>Prato</term><term>Racemic mixture</term><term>Scorrano</term><term>Side chain</term><term>Stationary phase</term><term>Stereoselective synthesis</term><term>Structural studies</term><term>Tertiary amide bond</term><term>Tetrahedron lett</term><term>Toluene solution</term><term>Toniolo</term><term>Trans equilibrium</term><term>Wudl</term></keywords></textClass></profileDesc></teiHeader><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. 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[45]</json:string><json:string>[2]</json:string><json:string>[57]</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-QSQD258K-8</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - chemistry, analytical</json:string><json:string>2 - biochemistry & molecular biology</json:string></wos><scienceMetrix><json:string>1 - health sciences</json:string><json:string>2 - biomedical research</json:string><json:string>3 - biophysics</json:string></scienceMetrix><scopus><json:string>1 - Physical Sciences</json:string><json:string>2 - Chemistry</json:string><json:string>3 - Organic Chemistry</json:string><json:string>1 - Life Sciences</json:string><json:string>2 - Pharmacology, Toxicology and Pharmaceutics</json:string><json:string>3 - Drug Discovery</json:string><json:string>1 - Life Sciences</json:string><json:string>2 - Pharmacology, Toxicology and Pharmaceutics</json:string><json:string>3 - Pharmacology</json:string><json:string>1 - 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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.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Fullerene‐based amino acids and peptides</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>FULLEROAMINO ACIDS AND PEPTIDES</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Fullerene‐based amino acids and peptides</title></titleInfo><name type="personal"><namePart type="given">Alberto</namePart><namePart type="family">Bianco</namePart><affiliation>Laboratoire de Chimie Immunologique, IBMC, UPR 9021 CNRS, Strasbourg, France</affiliation><affiliation>E-mail: A.Bianco@ibmc.u‐strasbg.fr</affiliation><affiliation>Correspondence address: Institut de Biologie Moléculaire et Cellulaire, UPR 9021 CNRS, 15, rue René Descartes, 67084 Strasbourg Cedex, France;</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Tatiana</namePart><namePart type="family">Da Ros</namePart><affiliation>Dipartimento di Scienze Farmaceutiche, Università di Trieste, Trieste, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Maurizio</namePart><namePart type="family">Prato</namePart><affiliation>Dipartimento di Scienze Farmaceutiche, Università di Trieste, Trieste, Italy</affiliation><affiliation>E-mail: prato@univ.trieste.it</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Claudio</namePart><namePart type="family">Toniolo</namePart><affiliation>Centro di Studio sui Biopolimeri, CNR, Dipartimento di Chimica Organica, Università di Padova, Padova, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="review-article" displayLabel="reviewArticle" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-L5L7X3NF-P">review-article</genre><originInfo><publisher>John Wiley & Sons, Ltd.</publisher><place><placeTerm type="text">Chichester, UK</placeTerm></place><dateIssued encoding="w3cdtf">2001-04</dateIssued><dateCaptured encoding="w3cdtf">2000-11-02</dateCaptured><dateValid encoding="w3cdtf">2000-11-04</dateValid><copyrightDate encoding="w3cdtf">2001</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">18</extent><extent unit="tables">0</extent><extent unit="references">71</extent></physicalDescription><abstract 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.</abstract><subject lang="en"><genre>keywords</genre><topic>fulleroamino acids</topic><topic>fulleropeptides</topic><topic>fulleroproline</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Peptide Science</title><subTitle>An Official Publication of the European Peptide Society</subTitle></titleInfo><titleInfo type="abbreviated"><title>J. 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