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Heterocyclic α-helix mimetics for targeting protein-protein interactions

The design and synthesis of α-helix peptidomimetics using inverse electron demand Diels-Alder reactions is described. The potency of the resulting pyridazine-based library to disrupt the Bak/Bcl-X(L) interaction was tested using an in vitro Fluorescence Polarization Assay.

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Bibliographische Detailangaben
Hauptverfasser: Biros, Shannon M., Moisan, Lionel, Mann, Enrique, Carella, Alexandre, Zhai, Dayong, Reed, John C., Rebek, Julius
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2007
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2699934/
https://ncbi.nlm.nih.gov/pubmed/17555961
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmcl.2007.05.075
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