Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Anne Bodlenner"'
Autor:
Marine Lafosse, Yan Liang, Jérémy P. Schneider, Elise Cartier, Anne Bodlenner, Philippe Compain, Marie-Pierre Heck
Publikováno v:
Molecules, Vol 27, Iss 15, p 4772 (2022)
Bambusurils, BU[4] and BU[6], were used for the first time as multivalent scaffolds to link glycosidases inhibitors derived from 1-deoxynojirimycin (DNJ). Two linear DNJ ligands having six or nine carbon alkyl azido linkers or a trivalent DNJ dendron
Externí odkaz:
https://doaj.org/article/741ad503dca44e4782347e1e609cb241
Autor:
Costanza Vanni, Anne Bodlenner, Marco Marradi, Jérémy P. Schneider, Maria de los Angeles Ramirez, Sergio Moya, Andrea Goti, Francesca Cardona, Philippe Compain, Camilla Matassini
Publikováno v:
Molecules, Vol 26, Iss 19, p 5864 (2021)
Among carbohydrate-processing enzymes, Jack bean α-mannosidase (JBα-man) is the glycosidase with the best responsiveness to the multivalent presentation of iminosugar inhitopes. We report, in this work, the preparation of water dispersible gold nan
Externí odkaz:
https://doaj.org/article/b0f7943841304d3aa05e7ba1014c5ec6
Autor:
Jérémy P. Schneider, Stefano Tommasone, Paolo Della Sala, Carmine Gaeta, Carmen Talotta, Céline Tarnus, Placido Neri, Anne Bodlenner, Philippe Compain
Publikováno v:
Pharmaceuticals, Vol 13, Iss 11, p 366 (2020)
A set of 6- to 24-valent clusters was constructed with terminal deoxynojirimycin (DNJ) inhibitory heads through C6 or C9 linkers by way of Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions between mono- or trivalent azido-armed iminosugars
Externí odkaz:
https://doaj.org/article/463ec6affc634d408ac87795bd8767ce
Autor:
Mathieu L. Lepage, Antoine Mirloup, Manon Ripoll, Fabien Stauffert, Anne Bodlenner, Raymond Ziessel, Philippe Compain
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 659-667 (2015)
The synthesis and photophysical properties of the first examples of iminosugar clusters based on a BODIPY or a pyrene core are reported. The tri- and tetravalent systems designed as molecular probes and synthesized by way of Cu(I)-catalysed azide–a
Externí odkaz:
https://doaj.org/article/3576c87ab1b0460890e55de08a5a4139
Autor:
Mathieu L. Lepage, Alessandra Meli, Anne Bodlenner, Céline Tarnus, Francesco De Riccardis, Irene Izzo, Philippe Compain
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1406-1412 (2014)
Cyclic N-propargyl α-peptoids of various sizes were prepared by way of macrocyclizations of linear N-substituted oligoglycines. These compounds were used as molecular platforms to synthesize a series of iminosugar clusters with different valency and
Externí odkaz:
https://doaj.org/article/3971cc530fb2483bb47ff3aa837b482e
Stereoselective Synthesis of Glycosyl Cyanides by TMSOTf‐Mediated Ring Opening of 1,6‐Anhydro Sugars
Publikováno v:
European Journal of Organic Chemistry. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::282ce381b75f772bc275756b287386ef
https://doi.org/10.1002/ejoc.202201311
https://doi.org/10.1002/ejoc.202201311
Autor:
Marco Marradi, Costanza Vanni, Maria de los Angeles Ramirez, Philippe Compain, Andrea Goti, Camilla Matassini, Sergio Moya, Francesca Cardona, Anne Bodlenner, Jérémy P. Schneider
Publikováno v:
Molecules
Volume 26
Issue 19
Molecules, Vol 26, Iss 5864, p 5864 (2021)
Volume 26
Issue 19
Molecules, Vol 26, Iss 5864, p 5864 (2021)
Among carbohydrate-processing enzymes, Jack bean α-mannosidase (JBα-man) is the glycosidase with the best responsiveness to the multivalent presentation of iminosugar inhitopes. We report, in this work, the preparation of water dispersible gold nan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a227f9b997146a31e731220cddc50f50
Publikováno v:
Organic & Biomolecular Chemistry. 17:5801-5817
The best multivalent effects observed in glycosidase inhibition have been achieved so far with jack bean α-mannosidase (JBα-man) using iminosugar clusters based on weakly binding mismatching active-site-directed inhibiting epitopes (inhitopes) in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::268d1851f82807d5f06cd095d0221452
https://doi.org/10.1039/c9ob00826h
https://doi.org/10.1039/c9ob00826h
Autor:
Paolo Della Sala, Carmen Talotta, Placido Neri, Stefano Tommasone, Céline Tarnus, Anne Bodlenner, Carmine Gaeta, Jérémy P. Schneider, Philippe Compain
Publikováno v:
Pharmaceuticals
Volume 13
Issue 11
Pharmaceuticals, Vol 13, Iss 366, p 366 (2020)
Volume 13
Issue 11
Pharmaceuticals, Vol 13, Iss 366, p 366 (2020)
A set of 6- to 24-valent clusters was constructed with terminal deoxynojirimycin (DNJ) inhibitory heads through C6 or C9 linkers by way of Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions between mono- or trivalent azido-armed iminosugars
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f8e7a414689b9432b2661f9db6faf28