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Fragment-based and structure-guided discovery of perforin inhibitors.

Eur J Med Chem 261: 0-0 (2023)
University of Auckland
Design, synthesis and biological evaluation of novel 2,4-thiazolidinedione derivatives able to target the human BAG3 protein.

Eur J Med Chem 261: 0-0 (2023)
Aptuit An Evotec
Chemical exploration of TGR5 functional hot-spots: Synthesis and structure-activity relationships of C7- and C23-Substituted cholic acid derivatives.

Eur J Med Chem 261: 0-0 (2023)
Tes Pharma
PITB: A high affinity transthyretin aggregation inhibitor with optimal pharmacokinetic properties.

Eur J Med Chem 261: 0-0 (2023)
Autonomous University of Barcelona
Discovery of novel multifunctional ligands targeting GABA transporters, butyrylcholinesterase, β-secretase, and amyloid β aggregation as potential treatment of Alzheimer's disease.

Eur J Med Chem 261: 0-0 (2023)
Jagiellonian University Medical College