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Tackle undruggable targets by screening for binary and ternary PROTAC interactions using Dianthus

Learn how you can trust Dianthus to efficiently evaluate the binary and ternary complex formed by PROTACs, ubiquitin ligase, and the protein of interest.

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Going small to win big: Fragment-based screening in drug discovery
Going small to win big: Fragment-based screening in drug discovery

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3 case studies on how to characterize challenging drug discovery targets — membrane proteins, peptide libraries, and PROTACs
3 case studies on how to characterize challenging drug discovery targets — membrane proteins, peptide libraries, and PROTACs

A caveat to a successful pharmaceutical industry in which many effective drugs have already been discovered...

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