Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Serge, Sablé"'
Autor:
Camille, Doyen, Eric, Larquet, Pierre-Damien, Coureux, Oriane, Frances, Frédéric, Herman, Serge, Sablé, Jean-Pierre, Burnouf, Christina, Sizun, Ewen, Lescop
Publikováno v:
Molecular pharmaceutics. 18(7)
Liposomal formulations represent attractive biocompatible and tunable drug delivery systems for peptide drugs. Among the tools to analyze their physicochemical properties, nuclear magnetic resonance (NMR) spectroscopy, despite being an obligatory tec
Autor:
Jean-Pierre Burnouf, Christina Sizun, Frédéric Herman, Eric Larquet, Pierre-Damien Coureux, Camille Doyen, Serge Sablé, Oriane Frances, Ewen Lescop
Publikováno v:
Molecular Pharmaceutics
Molecular Pharmaceutics, American Chemical Society, 2021, 18 (7), pp.2521-2539. ⟨10.1021/acs.molpharmaceut.1c00037⟩
Molecular Pharmaceutics, American Chemical Society, 2021, 18 (7), pp.2521-2539. ⟨10.1021/acs.molpharmaceut.1c00037⟩
International audience; Liposomal formulations represent attractive biocompatible and tunable drug delivery systems for peptide drugs. Among the tools to analyze their physicochemical properties, nuclear magnetic resonance (NMR) spectroscopy, despite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::077d705878432ed57490cf6af99f9756
https://hal.archives-ouvertes.fr/hal-03301899/document
https://hal.archives-ouvertes.fr/hal-03301899/document
Autor:
Simon Specklin, Camille Lecourt, Georges Massiot, Janine Cossy, Geoffroy Sorin, Christophe Meyer, Eric Auclair, Etienne Fleury, Antonio Grondin, Khalil Yamani, Karim Hammad, François Sautel, Paola B. Arimondo, Janick Ardisson, Marie-Isabelle Lannou, Sabrina Dhambri, Serge Sablé, Guillaume Boissonnat
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2019, 25 (11), pp.2745-2749. ⟨10.1002/chem.201806327⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2019, 25 (11), pp.2745-2749. ⟨10.1002/chem.201806327⟩
International audience; A strategy for the assembly of the entire carbon backbone of a stereoisomer of the antitumor marine natural product hemicalide has been investigated. The devised convergent approach relies on Horner–Wadsworth–Emmons and Ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7df7729a2c0fd815fe46c6aed4a8730
https://hal.archives-ouvertes.fr/hal-02379818
https://hal.archives-ouvertes.fr/hal-02379818
Autor:
Martin Gerlitz, Serge Sablé, Joachim Wink, Antje Nußer, Helene Olivan, Winfried Heyse, Herbert Kogler, Mark Brönstrup, Astrid Rey, Cedric Couturier, Luigi Toti, Michael Kurz, Armin Bauer, Cosima Dufour
Publikováno v:
Chemistry - A European Journal. 18:16123-16128
In an antibiotic lead discovery program, the known strain Streptomyces armeniacus DSM19369 has been found to produce three new natural products when cultivated on a malt-containing medium. The challenging structural elucidation of the isolated compou
Publikováno v:
The Journal of Organic Chemistry. 75:5151-5163
Synthetic studies toward the spiroketal core of spirangien A are described. Two synthetic approaches were developed. Both of them use a diastereoselective aldol addition of a lithium enolate derived from a methyl ketone on an aldehyde. In the first a
Autor:
Georges Bashiardes, Jean-Christophe Gueguen, Bruno Filoche, Jean-Christophe Carry, Marc Vuilhorgne, Serge Mignani, Jean-Claude Barriere, Claude Bensoussan, Serge Sablé, Norbert Dereu, Michel Evers
Publikováno v:
Scopus-Elsevier
A regio- and stereoselective synthesis of original semisynthetic di- and tri-functionalized non-immunosuppressive cyclosporins by way of a Barton ester decarboxylation and a C-thioalkylation starting from cyclosporin A (CsA) and [4'-hydroxy-MeLeu] 4
Autor:
Jean-Christophe Carry, Georges Bashiardes, Serge Mignani, Marc Vuilhorgne, Yvette Henin, Serge Sablé, Norbert Dereu, Jean-Claude Barriere, Anne Bousseau, Bruno Filoche, Michel Evers
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 13:4415-4419
Original cyclosporin A (CsA) derivatives bearing various alkylthio side chains at the sarcosine residue 3 (R configuration) and for the most potent and selective compounds a 4'-hydroxyl group at the Me-Leucine residue 4 were prepared in one or two st
Autor:
Richard Labaudiniere, Marc Vuilhorgne, Gilles Doerflinger, Serge Mignani, Serge Sablé, Guy Pantel, Jean-Pierre Leconte, Dominique Damour
Publikováno v:
Synlett. 1999:189-192
Autor:
Dominique Damour, Gilles Doerflinger, Serge Sablé, Serge Mignani, Richard Labaudiniere, Marc Vuilhorgne, Jean-Pierre Leconte, Guy Pantel
Publikováno v:
ChemInform. 30