In Silico Improvement of β3-Peptide Inhibitors of p53•hDM2 and p53•hDMX
Author:
Affiliation:
1. Departments of Chemistry and Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520-8107
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja901478e
Reference30 articles.
1. Inhibiting the p53–MDM2 interaction: an important target for cancer therapy
2. Targeting the MDM2-p53 Interaction for Cancer Therapy
3. A Rapid Library Screen for Tailoring β-Peptide Structure and Function
4. Helical β-Peptide Inhibitors of the p53-hDM2 Interaction
5. β-Peptides with improved affinity for hDM2 and hDMX
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