Bioorganic and Medicinal Chemistry Letters p. 1677 - 1682 (1996)
Update date:2022-08-04
Topics:
Steinmetzer, Torsten
Konishi, Yasuo
Several substituted methyl ketone derivatives of tripeptides with a C-terminal arginyl residue were synthesized as active site inhibitors of human α-thrombin. The most active compound among this series was the pyridinium methyl ketone D-Cha-Pro-Arg-PMK, w
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Doi:10.1007/BF00906819
()Doi:10.1016/0022-328X(96)06377-2
(1996)Doi:10.1039/cc9960001917
(1996)Doi:10.1039/j39680001232
(1968)Doi:10.1248/cpb.12.1446
(1964)Doi:10.1016/0960-894X(96)00354-X
(1996)
