15 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Novel Indazole Compounds as TEAD Inhibitors for Treating Cancer.

Smith, Gambrell & Russell
Novel Compounds as TEAD Inhibitors for Treating Cancer.

Smith, Gambrell & Russell
A chemical perspective on the modulation of TEAD transcriptional activities: Recent progress, challenges, and opportunities.

Shanghai Institute of Materia Medica
Small-Molecule Cyanamide Pan-TEAD·YAP1 Covalent Antagonists.

Indiana University
Diversity-oriented synthesis as a tool to expand the chemical space of DNA-encoded libraries.

University of Florence
Discovery of a selective and covalent small-molecule inhibitor of BFL-1 protein that induces robust apoptosis in cancer cells.

Yancheng Teachers University
Optimization of TEAD P-Site Binding Fragment Hit into In Vivo Active Lead

Merck Healthcare
Discovery of a cryptic site at the interface 2 of TEAD - Towards a new family of YAP/TAZ-TEAD inhibitors.

Lille Neuroscience and Cognition Research Center
Discovery of Covalent Inhibitors Targeting the Transcriptional Enhanced Associate Domain Central Pocket.

Max Planck Institute of Molecular Physiology
Structure-based design of potent linear peptide inhibitors of the YAP-TEAD protein-protein interaction derived from the YAP omega-loop sequence.

Novartis Institutes For Biomedical Research
Antiproliferative and Antimigratory Effects of a Novel YAP-TEAD Interaction Inhibitor Identified Using in Silico Molecular Docking.

University of Bristol
Discovery and biological evaluation of vinylsulfonamide derivatives as highly potent, covalent TEAD autopalmitoylation inhibitors.

Shanghai Institute of Materia Medica
Targeting Transcriptional Enhanced Associate Domains (TEADs).

Universities of Lille
PYRAZOLYL DERIVATIVES AS INHIBITORS OF THE KRAS MUTANT PROTEIN

Novartis
UNIT DOSAGE COMPOSITION OF AKT INHIBITOR

Nanjing Chia Tai Tianqing Pharmaceutical