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In silico improvement of β(3)-peptide inhibitors of p53•hDM2 and p53•hDMX

There is great interest in molecules capable of inhibiting the interactions between p53 and its negative regulators hDM2 and hDMX, as these molecules have validated potential against cancers in which one or both oncoproteins are overexpressed. We reported previously that appropriately substituted β(...

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Détails bibliographiques
Auteurs principaux: Michel, Julien, Harker, Elizabeth A., Tirado-Rives, Julian, Jorgensen, William L., Schepartz, Alanna
Format: Artigo
Langue:Inglês
Publié: 2009
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2754742/
https://ncbi.nlm.nih.gov/pubmed/19415930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja901478e
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