Abstract:The Front Cover shows new macrocyclic plasmin inhibitors containing a C‐terminal P1 benzylamine group. Their N‐terminal substitution provided analogues with sub‐nanomolar Ki values. Additional inhibitors containing an asymmetric linker possess Ki values close to 2 nM. For the first time, crystal structures of these macrocyclic inhibitors in complex with a Ser195Ala microplasmin mutant were determined, which explain their excellent potency and selectivity. More information can be found in the Research Article b… Show more
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