Tripeptidyl pyridinium methyl ketones as potent active site inhibitors of thrombin
摘要:
Several substituted methyl ketone derivatives of tripeptides with a C-terminal arginyl residue were synthesized as active site inhibitors of human alpha-thrombin. The most active compound among this series was the pyridinium methyl ketone D-Cha-Pro-Arg-PMK, which was characterized as a slow-binding inhibitor with a K-i of 0,19 nM. Copyright (C) 1996 Elsevier Science Ltd
Tripeptidyl pyridinium methyl ketones as potent active site inhibitors of thrombin
摘要:
Several substituted methyl ketone derivatives of tripeptides with a C-terminal arginyl residue were synthesized as active site inhibitors of human alpha-thrombin. The most active compound among this series was the pyridinium methyl ketone D-Cha-Pro-Arg-PMK, which was characterized as a slow-binding inhibitor with a K-i of 0,19 nM. Copyright (C) 1996 Elsevier Science Ltd