14 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Discovery of Selective Small-Molecule Inhibitors for theß-Catenin/T-Cell Factor Protein-Protein Interaction through the Optimization of the Acyl Hydrazone Moiety.

University of Utah
Hot spot-based design of small-molecule inhibitors for protein-protein interactions.

University of Utah
Direct targeting ofß-catenin: Inhibition of protein-protein interactions for the inactivation of Wnt signaling.

Chemical Genomics Centre of The Max Planck Society
Design, synthesis, and biological evaluation of novel 8-substituted quercetin derivatives targeting the β‑catenin/B-cell lymphoma 9 interaction.

Tongji University
Design, synthesis and biological evaluation of quercetin derivatives as novel β-catenin/B-cell lymphoma 9 protein-protein interaction inhibitors.

Fudan University
Recent advances of β-catenin small molecule inhibitors for cancer therapy: Current development and future perspectives.

Sichuan University
Discovery of Novel 3-Phenylpiperidine Derivatives Targeting the β-Catenin/B-Cell Lymphoma 9 Interaction as a Single Agent and in Combination with the Anti-PD-1 Antibody for the Treatment of Colorectal Cancer.

Fudan University
Small-Molecule Inhibitors Targeting the Canonical WNT Signaling Pathway for the Treatment of Cancer.

Ocean University of China
Targeting the interaction of β-catenin and TCF/LEF transcription factors to inhibit oncogenic Wnt signaling.

Vu University Amsterdam
Biophysical Survey of Small-Molecule β-Catenin Inhibitors: A Cautionary Tale.

University of Southampton
Discovery of an Orally Bioavailable Small-Molecule Inhibitor for the β-Catenin/B-Cell Lymphoma 9 Protein-Protein Interaction.

H. Lee Moffitt Cancer Center and Research Institute
Enhancing the Cell Permeability of Stapled Peptides with a Cyclic Cell-Penetrating Peptide.

The Ohio State University
Optimization of Peptidomimetics as Selective Inhibitors for the β-Catenin/T-Cell Factor Protein-Protein Interaction.

H. Lee Moffitt Cancer Center and Research Institute
Substituted B-amino acid derivatives as CXCR3 receptor antagonists

Sanofi