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FEBS Letters|October 6, 2000
Epoxysuccinyl peptide-derived affinity labels for cathepsin BN Schaschke, I Assfalg-Machleidt, T Lassleben, et al.Bioorganic & Medicinal Chemistry Letters|April 13, 2000
Beta-cyclodextrin/epoxysuccinyl peptide conjugates: a new drug targeting system for tumor cellsN Schaschke, I Assfalg-Machleidt, W Machleidt, et al.FEBS Letters|February 14, 1998
Substrate/propeptide-derived endo-epoxysuccinyl peptides as highly potent and selective cathepsin B inhibitorsN Schaschke, I Assfalg-Machleidt, W Machleidt, et al.Bioorganic & Medicinal Chemistry|November 14, 1997
E-64 analogues as inhibitors of cathepsin B. On the role of the absolute configuration of the epoxysuccinyl groupN Schaschke, I Assfalg-Machleidt, W Machleidt, et al.FEBS Letters|August 12, 1996
Cyclodextrins as templates for the presentation of protease inhibitorsN Schaschke, H J Musiol, I Assfalg-Machleidt, et al.Current Pharmaceutical Design|February 23, 2007
Mast cell tryptase beta as a target in allergic inflammation: an evolving storyC P Sommerhoff, N SchaschkeBiological Chemistry Hoppe-Seyler|May 1, 1988
Enzymatically active cathepsin B dissociating from its inhibitor complexes is elevated in blood plasma of patients with septic shock and some malignant tumorsI Assfalg-Machleidt, M Jochum, W Klaubert, et al.Biomedica Biochimica Acta|January 1, 1991
Proteolysis of defensive proteins in peritonitis exudate: pathobiochemical aspects and therapeutical approachA Billing, D Fröhlich, I Assfalg-Machleidt, et al.The Journal of Biological Chemistry|September 5, 1988
Proteinase-sensitive regions in the heavy chain of low molecular weight kininogen map to the inter-domain junctionsR Vogel, I Assfalg-Machleidt, A Esterl, et al.Biomedica Biochimica Acta|January 1, 1991
Molecular mechanism of inhibition of cysteine proteinases by their protein inhibitors: kinetic studies with natural and recombinant variants of cystatins and stefinsW Machleidt, U Thiele, I Assfalg-Machleidt, et al.Pageof 31