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Oznake: 3CLpro inhibitors;covalent inhibitors;fragment linking;fragment-based drug discovery;
Linking of fragments in neighboring binding sites is one of the optimization strategies in fragment-based drug discovery, where additive or even more substantial bioactivity improvements can be realized. However, such efforts present a considerable challenge when one fragment binds covalently to the ...
Leto: 2026 Vir: Fakulteta za farmacijo (UL FFA)
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