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Results: 1-8 |
Results: 8
Pseudopeptides containing the 2-hydrazonoacyl fragment: analogs of the chemotactic agent HCO-Met-Leu-Phe-OMe
Authors: Torrini, I Nalli, M Paradisi, MP Zecchini, GP Lucente, G Spisani, S
Citation: I. Torrini et al., Pseudopeptides containing the 2-hydrazonoacyl fragment: analogs of the chemotactic agent HCO-Met-Leu-Phe-OMe, J PEPT RES, 58(1), 2001, pp. 56-66
Bioactive fMLF-OMe analogs containing a N-terminal oximic or formylhydrazonic moiety
Authors: Torrini, I Paradisi, MP Zecchini, GP Lucente, G Mastropietro, G Spisani, S
Citation: I. Torrini et al., Bioactive fMLF-OMe analogs containing a N-terminal oximic or formylhydrazonic moiety, J PEPT RES, 55(2), 2000, pp. 102-109
4-amino-1,2-dithiolane-4-carboxylic acid (Adt) as cysteine conformationally restricted analogue. Synthetic protocol for Adt containing peptides
Authors: Morera, E Nalli, M Pinnen, F Rossi, D Lucente, G
Citation: E. Morera et al., 4-amino-1,2-dithiolane-4-carboxylic acid (Adt) as cysteine conformationally restricted analogue. Synthetic protocol for Adt containing peptides, BIOORG MED, 10(14), 2000, pp. 1585-1588
Biscarbamate analogues of the chemotactic tripeptide fMLF-OMe
Authors: Zecchini, GP Paradisi, MP Torrini, I Nalli, M Lucente, G Spisani, S
Citation: Gp. Zecchini et al., Biscarbamate analogues of the chemotactic tripeptide fMLF-OMe, FARMACO, 55(4), 2000, pp. 308-313
Peptides containing the sulfonamide junction. 2. Structure and conformation of Z-Tau-Pro-D-Phe-NHiPr
Authors: Calcagni, A Gavuzzo, E Lucente, G Mazza, F Morera, E Paradisi, MP Rossi, D
Citation: A. Calcagni et al., Peptides containing the sulfonamide junction. 2. Structure and conformation of Z-Tau-Pro-D-Phe-NHiPr, BIOPOLYMERS, 54(6), 2000, pp. 379-387
Novel glutathione analogues containing the dithiol and disulfide form of the Cys-Cys dyad
Authors: Calcagni, A Lucente, G Luisi, G Pinnen, F Rossi, D
Citation: A. Calcagni et al., Novel glutathione analogues containing the dithiol and disulfide form of the Cys-Cys dyad, AMINO ACIDS, 17(3), 1999, pp. 257-265
Topographically constrained aromatic alpha-aza-amino acids. Part 2. New azaTic-containing peptides: Synthesis, conformation, and intramolecular NH center dot center dot center dot N interaction
Authors: Torrini, I Zecchini, GP Paradisi, MP Mastropietro, G Lucente, G Gavuzzo, E Mazza, F
Citation: I. Torrini et al., Topographically constrained aromatic alpha-aza-amino acids. Part 2. New azaTic-containing peptides: Synthesis, conformation, and intramolecular NH center dot center dot center dot N interaction, TETRAHEDRON, 55(7), 1999, pp. 2077-2090
Design and synthesis of glutathione analogues
Authors: Lucente, G Luisi, G Pinnen, F
Citation: G. Lucente et al., Design and synthesis of glutathione analogues, FARMACO, 53(12), 1998, pp. 721-735
Risultati: 1-8 |