Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Muriel Pipelier"'
Autor:
Aline Pillot, Alain Defontaine, Amina Fateh, Annie Lambert, Maruthi Prasanna, Mathieu Fanuel, Muriel Pipelier, Noemi Csaba, Typhaine Violo, Emilie Camberlein, Cyrille Grandjean
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
Glycoconjugate vaccines are formed by covalently link a carbohydrate antigen to a carrier protein whose role is to achieve a long lasting immune response directed against the carbohydrate antigen. The nature of the sugar antigen, its length, its rati
Externí odkaz:
https://doaj.org/article/f04f8db38ce444cb962c698baea28091
Autor:
Katy Akoumany, Agata Zykwinska, Corinne Sinquin, Laëtitia Marchand, Mathieu Fanuel, David Ropartz, Hélène Rogniaux, Muriel Pipelier, Christine Delbarre-Ladrat, Sylvia Colliec-Jouault
Publikováno v:
Molecules, Vol 24, Iss 19, p 3441 (2019)
Bacteria from deep-sea hydrothermal vents constitute an attractive source of bioactive molecules. In particular, exopolysaccharides (EPS) produced by these bacteria become a renewable source of both biocompatible and biodegradable molecules. The low
Externí odkaz:
https://doaj.org/article/9fc048a62d3d4989a3c79393868903ea
Autor:
Eric Léonel, Morgane Rousselle, Didier Dubreuil, Gervaise Loirand, Florian Dilasser, Rémy Le Guével, Erwan Le Gall, Muriel Pipelier, Vincent Sauzeau, Stéphane Sengmany, Jacques Lebreton, Mathilde Sitter, Thierry Martens
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic and Medicinal Chemistry Letters, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic & Medicinal Chemistry Letters
Bioorganic & Medicinal Chemistry Letters, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic and Medicinal Chemistry Letters, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
Bioorganic & Medicinal Chemistry Letters
Bioorganic & Medicinal Chemistry Letters, 2019, 29 (5), pp.755-760. ⟨10.1016/j.bmcl.2018.12.050⟩
International audience; Various 3-amino-, 3-aryloxy- and alkoxy-6-arylpyridazines have been synthesized by an electrochemical reductive cross-coupling between 3-amino-, 3-aryloxy- or 3-alkoxy-6-chloropyridazines and aryl or heteroaryl halides. In vit
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 6, Pp o938-o939 (2013)
The title compound, C15H20O5, presents a bisnorsesquiterpene skeleton, with a trans-decaline backbone constrained by the lactone bridge. The α-hydroxy substituent and the methyl group belonging to the two decaline rings are in axial positions, where
Externí odkaz:
https://doaj.org/article/b07c5fa869a344f2ad0878f781d2c206
Autor:
Arnaud Martel, Florian Rouzier, Stéphane Guillarme, Gilles Dujardin, Rosanne Sillé, Arnaud Tessier, Arnaud Nourry, Muriel Pipelier, Ophélie Montiège
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2020, ⟨10.1002/ejoc.202001162⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2020, ⟨10.1002/ejoc.202001162⟩
International audience; An efficient two-step strategy for the synthesis of constrained C-glycosyl amino acid derivatives from C-vinylglycosides involving a 1,3-dipolar cycloaddition using L-(-)menthone-derived nitrone as the key step is described. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22a9ea68c9d9c3dce5639fed2eda9069
https://hal.archives-ouvertes.fr/hal-03085851
https://hal.archives-ouvertes.fr/hal-03085851
Autor:
Sana Kouba, Monique Mathé-Allainmat, Paul-Alain Jaffrès, Christophe Vandier, Muriel Pipelier, Aurélie Chantôme, Jacques Lebreton, Didier Dubreuil, Xuexin Zhang, Marie Potier-Cartereau, Mohamed Trebak, Romain Félix, Julien Braire
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2020, 186, pp.111854. ⟨10.1016/j.ejmech.2019.111854⟩
European Journal of Medicinal Chemistry, 2020, 186, pp.111854. ⟨10.1016/j.ejmech.2019.111854⟩
European Journal of Medicinal Chemistry, Elsevier, 2020, 186, pp.111854. ⟨10.1016/j.ejmech.2019.111854⟩
European Journal of Medicinal Chemistry, 2020, 186, pp.111854. ⟨10.1016/j.ejmech.2019.111854⟩
International audience; Small Conductance Calcium (Ca 2-)-activated potassium (K-) channels (SKCa) are now proved to be involved in many cancer cell behaviors such as proliferation or migration. The SIG channel isoform was particularly described in b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4939da4e9cd31fe372dae955ef49c6f8
https://hal.univ-brest.fr/hal-02441673
https://hal.univ-brest.fr/hal-02441673
Autor:
Hélène Rogniaux, Katy Akoumany, David Ropartz, Sylvia Colliec-Jouault, Christine Delbarre-Ladrat, Laëtitia Marchand, Mathieu Fanuel, Muriel Pipelier, Corinne Sinquin, Agata Zykwinska
Publikováno v:
Molecules (1420-3049) (MDPI AG), 2019-10, Vol. 24, N. 19, P. 3441 (15p.)
Molecules
Molecules, MDPI, 2019, 24 (19), pp.1-15. ⟨10.3390/molecules24193441⟩
Molecules, Vol 24, Iss 19, p 3441 (2019)
Volume 24
Issue 19
Molecules
Molecules, MDPI, 2019, 24 (19), pp.1-15. ⟨10.3390/molecules24193441⟩
Molecules, Vol 24, Iss 19, p 3441 (2019)
Volume 24
Issue 19
Bacteria from deep-sea hydrothermal vents constitute an attractive source of bioactive molecules. In particular, exopolysaccharides (EPS) produced by these bacteria become a renewable source of both biocompatible and biodegradable molecules. The low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::851244f29a5fe92ca149d25e4d9f392d
https://archimer.ifremer.fr/doc/00515/62644/
https://archimer.ifremer.fr/doc/00515/62644/
Autor:
Arnaud Nourry, Florian Rouzier, Rosanne Sillé, Stéphane Guillarme, Arnaud Tessier, Muriel Pipelier
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2019, 51 (12), pp.2484-2488. ⟨10.1055/s-0037-1611800⟩
SYNTHESIS, Georg Thieme Verlag, 2019, 52 (12), pp.2484-2488. ⟨10.1055/s-0037-1611800⟩
SYNTHESIS, Georg Thieme Verlag, 2019, 51 (12), pp.2484-2488. ⟨10.1055/s-0037-1611800⟩
SYNTHESIS, Georg Thieme Verlag, 2019, 52 (12), pp.2484-2488. ⟨10.1055/s-0037-1611800⟩
The synthesis C-vinyl glycosides, useful intermediates for the synthesis of C-glycoconjugates, was carried out on gram-scale by controlled reduction of the corresponding ethynyl derivatives in good to excellent yields in different carbohydrate series
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::615844851d2b6382139d557cde78b53a
https://hal.archives-ouvertes.fr/hal-03086861
https://hal.archives-ouvertes.fr/hal-03086861
Autor:
Arnaud Tessier, Jézabel Rocher, Katy Akoumany, Allan Patinec, Virginie Blot, Didier Dubreuil, Jacques Le Pendu, Jean-Yves Le Questel, Bruno Linclau, Samuel Golten, Jérôme Graton, Muriel Pipelier, Denis Jacquemin, J.Y. Douillard, Jacques Lebreton
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2019, 178, pp.195-213. ⟨10.1016/j.ejmech.2019.05.069⟩
European Journal of Medicinal Chemistry, Elsevier, 2019, 178, pp.195-213. ⟨10.1016/j.ejmech.2019.05.069⟩
20 iNKT cells recognize CD1d/-galactosylceramide (-GalCer) complexes via their invariant 21 TCR receptor and stimulate the immune response. Many -GalCer analogues have been 22 investigated to interrogate this interaction. Following our previ
Autor:
Arnaud Tessier, Antoni Llobet, Jordi Benet-Buchholz, Mehmed Z. Ertem, Jacques Lebreton, Muriel Pipelier, Roc Matheu, Xavier Sala, Didier Dubreuil
Publikováno v:
ACS Catalysis
ACS Catalysis, American Chemical Society, 2018, 8 (3), pp.2039-2048. ⟨10.1021/acscatal.7b03638⟩
ACS Catalysis, 2018, 8 (3), pp.2039-2048. ⟨10.1021/acscatal.7b03638⟩
ACS Catalysis, American Chemical Society, 2018, 8 (3), pp.2039-2048. ⟨10.1021/acscatal.7b03638⟩
ACS Catalysis, 2018, 8 (3), pp.2039-2048. ⟨10.1021/acscatal.7b03638⟩
A family of Ru complexes based on the pentadentate ligand t5a(3-) ((2,5-bis(6-carboxylatopyridin-2-yl)pyrrol-1-ide) and pyridine (py) that includes \Ru-II(Ht5a-kappa-(NO)-O-2)(py)(3)\ (1H(II)(kappa-(NO)-O-2)), \Ru-III(t5a-kappa-(NO1.5)-O-3)(py)(2)\ (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5012afee4c19c91cbb426102a72a1c16
https://hal.archives-ouvertes.fr/hal-02141008
https://hal.archives-ouvertes.fr/hal-02141008