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dc.contributor.authorPohlmann, Adriana Raffinpt_BR
dc.contributor.authorQuirion, Jean-Charlespt_BR
dc.contributor.authorGuillaume, Dominiquept_BR
dc.contributor.authorHusson, Henri-Philippept_BR
dc.date.accessioned2013-07-03T01:42:37Zpt_BR
dc.date.issued1999pt_BR
dc.identifier.issn0100-4042pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/72962pt_BR
dc.description.abstractConformational constraint is an approach which can be used to restrict the flexibility of peptide molecules and to provide information on the topographical requirements of receptors. The incorporation of conformationally constrained units in a peptide can lead to peptide analogues that present numerous advantages such as the potentialization of the pharmacological activity and the decrease of enzymatic degradation. This review discusses the peptide analogues containing a lactam or azalactam unit in their sequences. Of particular interest has been the replacement of a dipeptide motif in a peptide that simulates a β-turn.en
dc.format.mimetypeapplication/pdf
dc.language.isoporpt_BR
dc.relation.ispartofQuimica Nova. Sao Paulo, S.P. Vol. 22, n. 6 (nov./dez. 1999), p. 828-837pt_BR
dc.rightsOpen Accessen
dc.subjectPeptídeospt_BR
dc.subjectPeptide analoguesen
dc.subjectConformational constrainten
dc.subjectAnalise conformacionalpt_BR
dc.subjectLactamen
dc.subjectAzalactamen
dc.subjectStructure-activityen
dc.titlePeptídeos de conformação restrita induzida pela incorporação de unidades (aza)lactâmicaspt_BR
dc.title.alternativeConformationally constrained induced peptides containing (aza)lactam units en
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000247420pt_BR
dc.type.originNacionalpt_BR


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