AAAAAA

   
Results: 1-14 |
Results: 14
Synthesis, activity on NK-(3) tachykinin receptor and conformational solution studies of scyliorhinin II analogs modified at position 16
Authors: Rodziewicz-Motowidlo, S Lesner, A Legowska, A Czaplewski, C Liwo, A Rolka, K Patacchini, R Quartara, L
Citation: S. Rodziewicz-motowidlo et al., Synthesis, activity on NK-(3) tachykinin receptor and conformational solution studies of scyliorhinin II analogs modified at position 16, J PEPT RES, 58(2), 2001, pp. 159-172
Cyclic analogue of human heat shock protein 70(29-42) fragment. Synthesis,conformational studies and evaluation of its immunogenicity
Authors: Karawajczyk, B Wirkus-Romanowska, I Wysocki, J Rolka, K Mackiewicz, Z Glosnicka, R Kupryszewski, G
Citation: B. Karawajczyk et al., Cyclic analogue of human heat shock protein 70(29-42) fragment. Synthesis,conformational studies and evaluation of its immunogenicity, POL J CHEM, 75(2), 2001, pp. 265-273
Low molecular mass inhibitors of bovine beta-trypsin containing binding loop fragment of CMTI-III. Synthesis and evaluation of inhibitory activity
Authors: Fraszczak, P Lis, K Jaskiewicz, A Miecznikowska, H Rolka, K Kupryszewski, G
Citation: P. Fraszczak et al., Low molecular mass inhibitors of bovine beta-trypsin containing binding loop fragment of CMTI-III. Synthesis and evaluation of inhibitory activity, POL J CHEM, 75(12), 2001, pp. 1863-1868
C-Terminal glycine is crucial for hyperalgesic activity of nociceptin/orphanin FQ-(1-6)
Authors: Kotlinska, J Suder, P Sciubisz, A Legowska, A Eilmes, J Rolka, K Silberring, J
Citation: J. Kotlinska et al., C-Terminal glycine is crucial for hyperalgesic activity of nociceptin/orphanin FQ-(1-6), EUR J PHARM, 419(1), 2001, pp. 33-37
Dynorphin A inhibits nociceptin-converting enzyme from the rat spinal cord
Authors: Suder, P Wade, D Legowska, A Kotlinska, J Rolka, K Silberring, J
Citation: P. Suder et al., Dynorphin A inhibits nociceptin-converting enzyme from the rat spinal cord, BIOC BIOP R, 287(4), 2001, pp. 927-931
Chromogenic substrates of bovine beta-trypsin: The influence of an amino acid residue in P1 position on their interaction with the enzyme
Authors: Lesner, A Kupryszewski, G Rolka, K
Citation: A. Lesner et al., Chromogenic substrates of bovine beta-trypsin: The influence of an amino acid residue in P1 position on their interaction with the enzyme, BIOC BIOP R, 285(5), 2001, pp. 1350-1353
Solution conformational study of Scyliorhinin I analogues with conformational constraints by two-dimensional NMR and theoretical conformational analysis
Authors: Rodziewicz-Motowidlo, S Legowska, A Qi, XF Czaplewski, C Liwo, A Sowinski, P Mozga, W Olczak, J Zabrocki, J Rolka, K
Citation: S. Rodziewicz-motowidlo et al., Solution conformational study of Scyliorhinin I analogues with conformational constraints by two-dimensional NMR and theoretical conformational analysis, J PEPT RES, 56(3), 2000, pp. 132-146
A comparison of solution conformations of scyliorhinin I and its analogue with N-methyl-L-phenylalanine in position 7
Authors: Klaudel, L Rodziewicz-Motowidlo, S Liwo, A Rolka, K
Citation: L. Klaudel et al., A comparison of solution conformations of scyliorhinin I and its analogue with N-methyl-L-phenylalanine in position 7, POL J CHEM, 74(8), 2000, pp. 1091-1099
Cyclic analogues of proline-rich protein fragments. Part III. Synthesis ofnew analogues, conformational studies and evaluation of immunotropic activity
Authors: Wirkus-Romanowska, I Rodziewicz-Motowidlo, S Miecznikowska, H Rolka, K Janusz, M Szymaniec, S Zablocka, A Fortuna, W Miedzybrodzki, R Lisowski, J Kupryszewski, G
Citation: I. Wirkus-romanowska et al., Cyclic analogues of proline-rich protein fragments. Part III. Synthesis ofnew analogues, conformational studies and evaluation of immunotropic activity, POL J CHEM, 74(8), 2000, pp. 1129-1141
Orphanin FQ/nociceptin inhibits morphine withdrawal
Authors: Kotlinska, J Suder, P Legowska, A Rolka, K Silberring, J
Citation: J. Kotlinska et al., Orphanin FQ/nociceptin inhibits morphine withdrawal, LIFE SCI, 66(8), 2000, pp. PL119-PL123
Design, chemical synthesis and kinetic studies of trypsin chromogenic substrates based on the proteinase binding loop of Cucurbita maxima trypsin inhibitor (CMTI-III)
Authors: Lesner, A Brzozowski, K Kupryszewski, G Rolka, K
Citation: A. Lesner et al., Design, chemical synthesis and kinetic studies of trypsin chromogenic substrates based on the proteinase binding loop of Cucurbita maxima trypsin inhibitor (CMTI-III), BIOC BIOP R, 269(1), 2000, pp. 81-84
Simplified analogue of Cucurbita maxima trypsin inhibitor III (CMTI-III) substituted with L-norleucine in position 8
Authors: Witczuk, B Fraszczak, P Jaskiewicz, A Lis, K Rolka, K Kupryszewski, G
Citation: B. Witczuk et al., Simplified analogue of Cucurbita maxima trypsin inhibitor III (CMTI-III) substituted with L-norleucine in position 8, POL J CHEM, 73(2), 1999, pp. 395-397
Cyclic analogues of proline-rich protein fragments. Part II: Conformational studies using NMR spectroscopy and theoretical conformational analysis
Authors: Rodziewicz, S Wirkus-Romanowska, I Ciurak, M Miecznikowska, H Kupryszewski, G Czaplewski, C Liwo, A Rolka, K
Citation: S. Rodziewicz et al., Cyclic analogues of proline-rich protein fragments. Part II: Conformational studies using NMR spectroscopy and theoretical conformational analysis, POL J CHEM, 73(10), 1999, pp. 1697-1710
Analogue of Cucurbita maxima trypsin inhibitor III (CMTI-III) with all L-cysteine residues substituted by L-penicillamine (Pen). synthesis and evaluation of trypsin inhibitory activity
Authors: Jaskiewicz, A Lesner, A Rozycki, J Kupryszewski, G Rolka, K
Citation: A. Jaskiewicz et al., Analogue of Cucurbita maxima trypsin inhibitor III (CMTI-III) with all L-cysteine residues substituted by L-penicillamine (Pen). synthesis and evaluation of trypsin inhibitory activity, POL J CHEM, 72(12), 1998, pp. 2537-2540
Risultati: 1-14 |