A hydrophilic residue at position 2 can improve specific biological responses in fMLP-OMe analogs.

Autor: Cavicchioni, G.¹, Spisani, S.²

Publikováno v: Journal of Peptide Research. Sep2001, Vol. 58 Issue 3, p257-262. 6p.

Ring-to-ring interconversion: a reactivity study of some substituted Z-phenylhydrazones of the 5-amino-3-benzoyl-1,2,4-oxadiazole

Autor: D'ANNA, Francesca, FRENNA, Vincenzo, MACALUSO, Gabriella, PACE, Vitalba, SPISANI S, SPINELLI D.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3658::f1702e004343fc488d75f01bb7125537
http://hdl.handle.net/10447/33330

Synthesis and bioactivity of chemotactic tetrapeptides: fMLF-OMe analogues incorporating spacer aminoacids at the lateral positions

Autor: Lucente G (Lucente, Gino), Giordano C (Giordano, Cesare), Sansone A (Sansone, Anna), Torino D (Torino, Domenica), Spisani S (Spisani, Susanna)

Publikováno v: Amino acids (Wien, Print) 37 (2009): 285–295.
info:cnr-pdr/source/autori:Lucente G (Lucente, Gino), Giordano C (Giordano, Cesare), Sansone A (Sansone, Anna), Torino D (Torino, Domenica), Spisani S (Spisani, Susanna)/titolo:Synthesis and bioactivity of chemotactic tetrapeptides: fMLF-OMe analogues incorporating spacer aminoacids at the lateral positions/doi:/rivista:Amino acids (Wien, Print)/anno:2009/pagina_da:285/pagina_a:295/intervallo_pagine:285–295/volume:37

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::15cbbec3ba283bae1f8e004a413da02b
http://www.cnr.it/prodotto/i/15938

Chemotactic tripeptides incorporating at position 2 á-aminoacid residues with unsaturated side chains

Autor: Lucente G., Paglialunga P.M., Giordano C., Sansone A., Torino D., Spisani S

Publikováno v: Amino acids (Wien, Print) (2007).
info:cnr-pdr/source/autori:Lucente G., Paglialunga P.M., Giordano C., Sansone A., Torino D. and Spisani S/titolo:Chemotactic tripeptides incorporating at position 2 á-aminoacid residues with unsaturated side chains/doi:/rivista:Amino acids (Wien, Print)/anno:2007/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::59debbe957d4773556264e2185cd2439
http://www.cnr.it/prodotto/i/15629

Formylpeptides trigger selective molecular pathways that are required in the physiological functions of human neutrophils

Autor: Selvatici, R. Falzarano S., Traniello S., Pagani Zecchini G., Spisani S.

Publikováno v: Cellular signalling 15 (2003): 377–383.
info:cnr-pdr/source/autori:Selvatici, R. Falzarano S., Traniello S., Pagani Zecchini G., Spisani S./titolo:Formylpeptides trigger selective molecular pathways that are required in the physiological functions of human neutrophils/doi:/rivista:Cellular signalling/anno:2003/pagina_da:377/pagina_a:383/intervallo_pagine:377–383/volume:15

For-Met-Delta(Z)Leu-Phe-OMe([Delta(Z)Leu(2)])is a conformationally restricted for-Met-Leu-Phe-OMe(fMLP-OMe) analogue able to descriminate between different responses of human neutrophils. In contrast, [Delta(Z)Leu(2)] significantly activates the tran

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::a86d19c9dfaca8d05e2fa7a5d154847c
http://www.cnr.it/prodotto/i/14854