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  • Cell surface ligands and receptors are the most valuable therapeutic targets, as more than one-third of all FDA-approved drugs targeting these proteins
  • Functional proteomics technologies are designed to identify intracellular protein-protein interaction networks but not ligand-receptor interactions
  • Our ligandomics is the only technology to globally identify cell-wide ligands with simultaneous binding activity quantification
  • Our Comparative ligandomics is the only technology for systematic map of disease-selective cellular ligands.
  • Therapies targeting disease-selective ligands have the advantages of high efficacy, minimal adverse side effects on normal cells, wide therapeutic windows, low drug attrition rates and reduced R&D costs.
Ligandomics technology globally identifies cell-wide ligands with simultaneous binding activity quantification. Comparative ligandomics quantitatively compares diseased cells vs. normal cells to systematically identify disease-selective ligands as high-quality drug targets for drug development.

 

 

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