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Results: 1-10 |
Results: 10
Structure-activity relationships of new NAPAP-analogs
Authors: Steinmetzer, T Schweinitz, A Kunzel, S Wikstrom, P Hauptmann, J Sturzebecher, J
Citation: T. Steinmetzer et al., Structure-activity relationships of new NAPAP-analogs, J ENZ INHIB, 16(3), 2001, pp. 241-249
Advances in the development of thrombin inhibitors
Authors: Steinmetzer, T Hauptmann, J Sturzebecher, J
Citation: T. Steinmetzer et al., Advances in the development of thrombin inhibitors, EXPERT OP I, 10(5), 2001, pp. 845-864
Synthesis and characterization of octapeptide somatostatin analogues with backbone cyclization: Comparison of different strategies, biological activities and enzymatic stabilities
Authors: Besser, D Muller, B Kleinwachter, P Greiner, G Seyfarth, L Steinmetzer, T Arad, O Reissmann, S
Citation: D. Besser et al., Synthesis and characterization of octapeptide somatostatin analogues with backbone cyclization: Comparison of different strategies, biological activities and enzymatic stabilities, J PRAK CHEM, 342(6), 2000, pp. 537-545
New bivalent thrombin inhibitors with N-alpha(methyl)arginine at the P1-position
Authors: Steinmetzer, T Batdordshjin, M Pineda, F Seyfarth, L Vogel, A Reissmann, S Hauptmann, J Sturzebecher, J
Citation: T. Steinmetzer et al., New bivalent thrombin inhibitors with N-alpha(methyl)arginine at the P1-position, BIOL CHEM, 381(7), 2000, pp. 603-610
Identification of novel periviscerokinins from single neurohaemal release sites in insects - MS/MS fragmentation complemented by Edman degradation
Authors: Predel, R Kellner, R Baggerman, G Steinmetzer, T Schoofs, L
Citation: R. Predel et al., Identification of novel periviscerokinins from single neurohaemal release sites in insects - MS/MS fragmentation complemented by Edman degradation, EUR J BIOCH, 267(12), 2000, pp. 3869-3873
New thrombin inhibitors based on D-Cha-Pro-derivatives
Authors: Steinmetzer, T Batdorsdhjin, M Kleinwachter, P Seyfarth, L Greiner, G Reissmann, S Sturzebecher, J
Citation: T. Steinmetzer et al., New thrombin inhibitors based on D-Cha-Pro-derivatives, J ENZ INHIB, 14(3), 1999, pp. 203-216
3-amidinophenylalanine-based inhibitors of urokinase
Authors: Sturzebecher, J Vieweg, H Steinmetzer, T Schweinitz, A Stubbs, MT Renatus, M Wikstrom, P
Citation: J. Sturzebecher et al., 3-amidinophenylalanine-based inhibitors of urokinase, BIOORG MED, 9(21), 1999, pp. 3147-3152
Two-stage method for protein-ligand docking
Authors: Hoffmann, D Kramer, B Washio, T Steinmetzer, T Rarey, M Lengauer, T
Citation: D. Hoffmann et al., Two-stage method for protein-ligand docking, J MED CHEM, 42(21), 1999, pp. 4422-4433
Potent bivalent thrombin inhibitors: Replacement of the scissile peptide bond at P-1-P-1 ' with arginyl ketomethylene isosteres
Authors: Steinmetzer, T Zhu, BY Konishi, Y
Citation: T. Steinmetzer et al., Potent bivalent thrombin inhibitors: Replacement of the scissile peptide bond at P-1-P-1 ' with arginyl ketomethylene isosteres, J MED CHEM, 42(16), 1999, pp. 3109-3115
Design and evaluation of novel bivalent thrombin inhibitors based on amidinophenylalanines
Authors: Steinmetzer, T Renatus, M Kunzel, S Eichinger, A Bode, W Wikstrom, P Hauptmann, J Sturzebecher, J
Citation: T. Steinmetzer et al., Design and evaluation of novel bivalent thrombin inhibitors based on amidinophenylalanines, EUR J BIOCH, 265(2), 1999, pp. 598-605
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