Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Soizic Besret"'
Autor:
Patricia Melnyk, Oleg Melnyk, Anthony Romieu, Hervé Drobecq, Fatima Dahmani, Rémi Desmet, Jérôme Vicogne, Véronique Fafeur, Soizic Besret
Publikováno v:
Bioconjugate Chemistry
The capacity of many proteins to interact with natural or synthetic polyanions has been exploited for modulating their biological action. However, the polydispersity of these macromolecular polyanions as well as their poor specificity is a severe lim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6497f259c08f7bd9ed5860e2f20feb61
https://doi.org/10.1021/bc500137j
https://doi.org/10.1021/bc500137j
Publikováno v:
Bioconjugate Chemistry
The design of novel chemoselective and site-specific ligation methods provides new tools for obtaining complex scaffolds, peptidomimetics, and peptide conjugates. The chemistry of the N-phenylthiocarbonyl group has led to several developments in pept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c68f1eb9026261c8c751495375bed90
https://doi.org/10.1021/bc500052r
https://doi.org/10.1021/bc500052r
Publikováno v:
Bioconjugate Chemistry. 20:1397-1403
Glycine is a amino acid frequently found in peptides. Substitution of a glycine residue by an azaglycine allows the modulation of peptide conformation, bioactivity, or stability. Azapeptides are usually prepared using solid-phase synthetic procedures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2006bc379b5a179fc141a0de87de5112
https://doi.org/10.1021/bc9000195
https://doi.org/10.1021/bc9000195
Publikováno v:
Journal of Peptide Science. 14:1244-1250
Peptide chemical ligation chemistries, which allow the chemoselective coupling of unprotected peptide fragments, are useful tools for synthesizing native polypeptides or unnatural peptide-based macromolecules. We show here that the phenylthiocarbonyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb6ee15a3e4726e42037742642a305c3
https://doi.org/10.1002/psc.1063
https://doi.org/10.1002/psc.1063
Publikováno v:
ChemInform. 45
The design of novel chemoselective and site-specific ligation methods provides new tools for obtaining complex scaffolds, peptidomimetics, and peptide conjugates. The chemistry of the N-phenylthiocarbonyl group has led to several developments in pept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9636138accba1d145a260602f15dc72c
https://doi.org/10.1002/chin.201422286
https://doi.org/10.1002/chin.201422286
Autor:
Françoise Martin-Nizard, Pascal Berthelot, Sébastien Dilly, Pascal Carato, Soizic Besret, Saïd Yous, Fariza Hadjaz, Philippe Chavatte, Patrick Duriez, Nicolas Lebegue
Publikováno v:
European journal of medicinal chemistry. 46(6)
A series of β-carboline compounds were synthesized, starting from compound GWC22, their antioxidant activity was determined by inhibition of lipid peroxidation. The oxidation of LDL was induced in the presence of CuSO4 or 2,2'-azobis(2-amidinopropan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21687cc11e1a1cfdeef9657a45ef7d38
https://pubmed.ncbi.nlm.nih.gov/21497423
https://pubmed.ncbi.nlm.nih.gov/21497423
Autor:
Soizic Besret, Jérôme Vicogne, Fatima Dahmani, Véronique Fafeur, Rémi Desmet, Hervé Drobecq, Anthony Romieu, Patricia Melnyk, Oleg Melnyk
Publikováno v:
Bioconjugate Chemistry; May2014, Vol. 25 Issue 5, p1000-1010, 11p