Building from of the well-understood cellular targeting abilities of antibodies, we combine the intrinsic efficiency of enzymes with the unique specificity of metal-free click chemistry to replace the native antibody glycan with a stably attached therapeutic payload.
Any antibody can be converted into a stably conjugated ADC in just a few days by modifying the native antibody glycan using our highly efficient enzymes and metal-free click chemistry approach.
Multiple independent experiments confirm that the native glycan position is likely one of the best for attaching ADC payloads to antibodies.
Differentiates ADC versus other site-specific ADC technologies
Multiple linker-payloads spanning various mechanisms of action
Protein-based molecules that recruit T and NK cells
toxSYN® Linker-Payload |
Mode-of-Action | Payload (Active Catabolite) |
---|---|---|
1. SYNtecan E™* | Topoisomerase 1 inhibitor | Camptothecin-based |
2. SYNeamicin D™* | DNA damaging agent |
Calicheamicin-based |
3. SYNeamicin G™* | ||
4. SYN-PNU™* | Nemorubicin-based | |
5. SYNstatin E™ | Microtubule inhibitors |
Auristatin-based |
6. SYNstatin F™ | ||
7. SYNtansine™ | Maytansine-based |
Bring your own and/or choose from the following categories.
Just like our ADC technology, we can easily attach peptide and protein-based payloads to your antibody.
Early preclinical data available on request.
NK cell recruitment
NK cell recruitment