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Our technology

Using engineered organisms, we can screen libraries of small molecules or libraries of DNA encoded peptides and macrocycles to identify compounds that can either disrupt a protein-protein interaction, or bridge an interaction.

Since the technology relies on a cell-based functional readout, we are able to discover compounds that work through either competitive or allosteric mechanisms. ​We can also engineer multiple readouts into one cell for complex functional modulation of difficult targets.

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