Potent Thrombin Inhibitors That Probe the S1‘ Subsite: Tripeptide Transition State Analogues Based on a Heterocycle-Activated Carbonyl Group

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Veröffentlicht in:	Journal of medicinal chemistry 1996-08, Vol.39 (16), p.3039-3043
Hauptverfasser:	Costanzo, Michael J, Maryanoff, Bruce E, Hecker, Leonard R, Schott, Mary R, Yabut, Stephen C, Zhang, Han-Cheng, Andrade-Gordon, Patricia, Kauffman, Jack A, Lewis, Joan M, Krishnan, Raman, Tulinsky, Alexander
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Sequence Animals Binding Sites Biological and medical sciences Blood. Blood coagulation. Reticuloendothelial system Cattle Crystallography, X-Ray Guanidines - chemical synthesis Guanidines - chemistry Guanidines - pharmacology Humans Medical sciences Molecular Sequence Data Molecular Structure Oligopeptides - pharmacology Peptides - chemical synthesis Peptides - chemistry Peptides - pharmacology Pharmacology. Drug treatments Pipecolic Acids - pharmacology Protein Binding Serine Proteinase Inhibitors - chemical synthesis Serine Proteinase Inhibitors - chemistry Serine Proteinase Inhibitors - pharmacology Thiazoles - chemical synthesis Thiazoles - chemistry Thiazoles - pharmacology Thrombin - antagonists & inhibitors Thrombin - chemistry Trypsin Inhibitors - chemical synthesis Trypsin Inhibitors - chemistry Trypsin Inhibitors - pharmacology
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