(N-acyl-N-alkyl)glycyl borolysine analogs: A new class of potent thrombin inhibitors

Abstract In this report the structure-activity relationships of a series of novel (N-acyl-N-alkyl)glycyl boro lysine thrombin inhibitors are described. This work culminates in the discovery of (N-3-phenylpropanoyl-N-phenethyl)glycyl boro lysine ( 12j ), a potent, orally active inhibitor with a binding conformation in which the N-phenethyl group occupies the aryl binding pocket of thrombin.