Synthesis, biological activity, conformational analysis by NMR and molecular modeling of N-formyl-L-Met-L-Pro-L-Phe-OMe, a praline analogue of the chemotactic peptide N-formyl-L-Met-L-Leu-L-Phe-OH
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1993.tb00482.x/fullpdf
Reference32 articles.
1. N-formylmethionyl peptides as chemoattractants for leucocytes.
2. Formyl peptide chemoattractants: a model of the receptor on rabbit neutrophils
3. Nuclear magnetic resonance conformational studies on the chemotactic tripeptide formyl-L-methionyl-L-leucyl-L-phenylalanine. A small .beta. sheet
4. Conformation and dynamics of the chemotactic peptide formyl-L-methionyl-L-leucyl-L-phenylalanine in solution
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1. Synthesis and bioactivity of chemotactic tetrapeptides: fMLF-OMe analogues incorporating spacer aminoacids at the lateral positions;Amino Acids;2008-07-18
2. Structure–activity relationship of for-l-Met l-Leu-l-Phe-OMe analogues in human neutrophils;Bioorganic Chemistry;2006-10
3. Hybrid α/β-peptides: For-Met-Leu-Phe-OMe analogues containing geminally disubstituted β2,2- and β3,3-amino acids at the central position;Amino Acids;2006-03-20
4. Hydrophilic residues at position 3 highlight unforeseen features of the fMLP receptor pocket;European Journal of Pharmacology;2003-05
5. The effect of the cyclopropyl group on the conformation of chemotactic formyl tripeptides;Bioorganic Chemistry;2003-04
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