Synthesis, conformation, and biological activity of two fMLP-OMe analogues containing the new 2-[2′-(methylthio) ethyl] methionine residue-Reference-Cited by-同舟云学术

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Synthesis, conformation, and biological activity of two fMLP-OMe analogues containing the new 2-[2′-(methylthio) ethyl] methionine residue

Published:1997-10-05 Issue:4 Volume:42 Page:415-426
ISSN:0006-3525
Container-title:Biopolymers
language:en
Short-container-title:Biopolymers

Author:

Torrini I.,Paradisi M. Paglialunga,Zecchini G. Pagani,Lucente G.,Gavuzzo E.,Mazza F.,Pochetti G.,Traniello S.,Spisani S.

Publisher

Wiley

Subject

Organic Chemistry,Biomaterials,Biochemistry,General Medicine,Biophysics

Reference44 articles.

1. Structures of polypeptides from α-amino acids disubstituted at the α-carbon

2. Non-standard amino acids in peptide design and protein engineering

3. Contrasting solution conformations of peptides containing ?,?-dialkylated residues with linear and cyclic side chains

4. New α-Amino Acids for Peptides of Biological Interest: 2-[2′-(Methylthio)Ethyl]Methionine Derivatives

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1. Chemotactic tripeptides incorporating at position 2 α-aminoacid residues with unsaturated side chains;Amino Acids;2007-12-28

2. Structure–activity relationship of for-l-Met l-Leu-l-Phe-OMe analogues in human neutrophils;Bioorganic Chemistry;2006-10

3. Chemotactic peptides: fMLF-OMe analogues incorporating proline–methionine chimeras as N-terminal residue;Bioorganic & Medicinal Chemistry;2006-04

4. 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

5. Conformational investigations on analogs of inflammation response inducing chemotactic tripeptide fMLP;Biopolymers;2005

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