Peptide argininol “inverse substrates” of anisic acid: Novel inhibitors of the trypsin-like serine proteinases
- 6 May 1997
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 7 (9) , 1133-1138
- https://doi.org/10.1016/s0960-894x(97)00174-1
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Design, Synthesis, and Evolution of a Novel, Selective, and Orally Bioavailable Class of Thrombin Inhibitors: P1-Argininal Derivatives Incorporating P3-P4 Lactam Sulfonamide MoietiesJournal of Medicinal Chemistry, 1996
- New coupling reagents in peptide chemistryTetrahedron Letters, 1989
- Convenient one-pot esterification of N-protected aminoacids via isopropenyl chloroformate activation.Tetrahedron Letters, 1987
- Coronary thrombolysis with intravenous anisoylated plasminogen-streptokinase complex BRL 26921.Heart, 1985
- The selective affinity labeling of factor Xa by peptides of arginine chloromethyl ketoneThrombosis Research, 1981
- Fibrinolysis with acyl-enzymes: a new approach to thrombolytic therapyNature, 1981
- [63] Inactivation of trypsin-like enzymes with peptides of arginine chloromethyl ketonePublished by Elsevier ,1981
- Proteolytic enzymes. 7. "Inverse substrates" for trypsin. Efficient enzymic hydrolysis of certain esters with a cationic center in the leaving groupJournal of the American Chemical Society, 1977
- Color test for detection of free terminal amino groups in the solid-phase synthesis of peptidesAnalytical Biochemistry, 1970
- Solid Phase Peptide Synthesis. I. The Synthesis of a TetrapeptideJournal of the American Chemical Society, 1963