ICE Bioscience Posters

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Fragment-based drug design (FBDD) has emerged as a powerful strategy in drug discovery, particularly for identifying novel scaffolds and binding sites for challenging targets. We have employed a combination of Spectral Shift and TR-FRET technologies to discover new molecular glue scaffolds. Our fragment library is diverse and includes a rich variety of E3 ligases from different species, providing a sustainable and versatile screening platform.


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