14 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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Design, synthesis and biological evaluation of PSMA/hepsin-targeted heterobivalent ligands.

Korea University
Design and Synthesis of Nonpeptide Inhibitors of Hepatocyte Growth Factor Activation.

Southern Research
Structure-based design, synthesis, and biological evaluation of Leu-Arg dipeptide analogs as novel hepsin inhibitors.

Korea University
Structure-guided discovery of 2-aryl/pyridin-2-yl-1H-indole derivatives as potent and selective hepsin inhibitors.

Aurigene Discovery Technologies
Structure-based discovery of small molecule hepsin and HGFA protease inhibitors: Evaluation of potency and selectivity derived from distinct binding pockets.

Washington University
Inhibitors of HGFA, Matriptase, and Hepsin Serine Proteases: A Nonkinase Strategy to Block Cell Signaling in Cancer.

Washington University
Design and synthesis of potent, selective inhibitors of matriptase.

TBA
Macrocyclic Inhibitors of HGF-Activating Serine Proteases Overcome Resistance to Receptor Tyrosine Kinase Inhibitors and Block Lung Cancer Progression.

Washington University School of Medicine
Discovery of Selective Matriptase and Hepsin Serine Protease Inhibitors: Useful Chemical Tools for Cancer Cell Biology.

Washington University School of Medicine
Multi-target compounds acting in cancer progression: Focus on thiosemicarbazone, thiazole and thiazolidinone analogues.

Universidade Federal De Pernambuco
Design, Synthesis, and Testing of Potent, Selective Hepsin Inhibitors via Application of an Automated Closed-Loop Optimization Platform.

University of Helsinki
Thienopyrimidones

Boehringer Ingelheim International
Pyrazolo[3,4-d]pyrimidine compounds, their preparation and use as sigma ligands

Laboratorios Del Dr. Esteve
Characterization of novel aryl-ether, biaryl, and fluorene aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT2.

Wyeth Research