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Designer macrocyclic organo-peptide hybrids inhibit the interaction between p53 and HDM2/X by accommodating a functional α-helix

We report the design of side-chain-to-tail linked organo-peptide hybrids incorporating an α-helical protein-binding motif. Using this strategy, macrocyclic inhibitors of the p53:HDM2 interaction displaying dual specificity against the HDMX homolog as well as increased proteolytic stability could be...

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Detalhes bibliográficos
Publicado no:Chem Commun (Camb)
Main Authors: Smith, Jessica M., Frost, John R., Fasan, Rudi
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4480681/
https://ncbi.nlm.nih.gov/pubmed/24710524
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c4cc01199f
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