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Journal Abstract Search
128 related items for PubMed ID: 10532239
1. An evaluation of fMLP pocket dimensions and features using formyltetrapeptides. Cavicchioni G, Varani K, Niccoli S, Rizzuti O, Spisani S. J Pept Res; 1999 Oct; 54(4):336-43. PubMed ID: 10532239 [Abstract] [Full Text] [Related]
2. Pseudopeptides containing the 2-hydrazonoacyl fragment: analogs of the chemotactic agent HCO-Met-Leu-Phe-OMe. Torrini I, Nalli M, Paglialunga Paradisi M, Pagani Zecchini G, Lucente G, Spisani S. J Pept Res; 2001 Jul; 58(1):56-66. PubMed ID: 11454170 [Abstract] [Full Text] [Related]
3. Biological variation responses in fMLP-OMe analogs, introducing bulky protecting groups on the side-chain of hydrophilic residues at position 2. Cavicchioni G, Turchetti M, Spisani S. J Pept Res; 2002 Oct; 60(4):223-31. PubMed ID: 12366529 [Abstract] [Full Text] [Related]
4. Synthesis and biological activity of a conformationally constrained chemotactic gamma-lactam formyl tetrapeptide. Cavicchioni G, Breveglieri A, Reali E, Spisani S. Arzneimittelforschung; 1996 Oct; 46(10):964-6. PubMed ID: 8931889 [Abstract] [Full Text] [Related]
5. Biological activity in human neutrophils of di-tripeptides, analogues of the chemotactic fMLP. Cavicchioni G, Turchetti M, Spisani S. Bioorg Med Chem Lett; 2001 Dec 17; 11(24):3157-9. PubMed ID: 11720864 [Abstract] [Full Text] [Related]
6. Biological activity of for-Met-Leu-Phe-OMe analogs: relevant substitutions specifically trigger killing mechanisms in human neutrophils. Cavicchioni G, Fraulini A, Turchetti M, Varani K, Falzarano S, Pavan B, Spisani S. Eur J Pharmacol; 2005 Apr 04; 512(1):1-8. PubMed ID: 15814083 [Abstract] [Full Text] [Related]
7. Isopeptide bonds in chemotactic tripeptides. Synthesis and activity of lysine-containing fMLF analogs. Pagani Zecchini G, Nalli M, Mollica A, Lucente G, Paglialunga Paradisi M, Spisani S. J Pept Res; 2002 Jun 04; 59(6):283-91. PubMed ID: 12010519 [Abstract] [Full Text] [Related]
8. A hydrophilic residue at position 2 can improve specific biological responses in fMLP-OMe analogs. Cavicchioni G, Spisani S. J Pept Res; 2001 Sep 04; 58(3):257-62. PubMed ID: 11576332 [Abstract] [Full Text] [Related]
9. Synthesis, biological activity, conformational analysis by NMR and molecular modeling of N-formyl-L-Met-L-Pro-L-Phe-OMe, a proline analogue of the chemotactic peptide N-formyl-L-Met-L-Leu-L-Phe-OH. Dugas H, Laroche M, Ptak M, Labbé H. Int J Pept Protein Res; 1993 Jun 04; 41(6):595-605. PubMed ID: 8394292 [Abstract] [Full Text] [Related]
16. Synthesis and biological evaluation of new active For-Met-Leu-Phe-OMe analogues containing para-substituted Phe residues. Mollica A, Feliciani F, Stefanucci A, Costante R, Lucente G, Pinnen F, Notaristefano D, Spisani S. J Pept Sci; 2012 Jun 04; 18(6):418-26. PubMed ID: 22528501 [Abstract] [Full Text] [Related]
17. The importance of the peptide bond at position 2 in HCO-Met-Leu-Phe-OMe analogues as shown by studies on human neutrophils. Cavicchioni G, Breveglieri A, Boggian M, Vertuani G, Reali E, Spisani S. J Pept Sci; 1996 Jun 04; 2(3):135-40. PubMed ID: 9231322 [Abstract] [Full Text] [Related]