Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anne Breteche"'
Publikováno v:
Tetrahedron. 66:4490-4494
An efficient synthesis of 3-amino-6-bromofuro[3,2-b]pyridine-2-carboxamides is described via the formation of 3-amino-6-bromofuro[3,2-b]pyridine-2-carbonitrile. Functionalization of the amino group at position 3 of the heterocycle will be discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73c16666a3827c0c62cdb9b62a7d6c7b
https://doi.org/10.1016/j.tet.2010.04.071
https://doi.org/10.1016/j.tet.2010.04.071
Autor:
J. Y. Petit, Morgane Lardic, Guillaume Le Baut, Anne Breteche, Muriel Duflos, Marie Renee Nourrisson, Alexandra Dassonville, N. Grimaud
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 23:728-738
In this study, the synthetic way to new N-pyridinyl(methyl)indolylpropanamides acting as non acidic NSAIDs has been described. Pharmacomodulation was carried out at N(1) and C(5) of the indole ring and at the level of the propanamide chain. N(3)-pyri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0f8b5b36953d6e70a9111640928b147
https://doi.org/10.1080/14756360802208251
https://doi.org/10.1080/14756360802208251
Autor:
Patrick Hautefaye, Marie-Renée Nourrisson, Pascal Marchand, Guillaume De Nanteuil, Anne Breteche, Muriel Duflos
Publikováno v:
ChemInform. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bedd2ef69b778491de3a6f84018a52c6
https://doi.org/10.1002/chin.201146159
https://doi.org/10.1002/chin.201146159
Autor:
Gaëtane Wielgosz-Collin, Claire Denis, Jean-Michel Kornprobst, Nicole Boury-Esnault, Vony Rabesaotra, Gilles Barnathan, Anne Breteche, Nicolas Ruiz
Publikováno v:
Lipids
Lipids, 2009, 44 (7), pp.655-663. ⟨10.1007/s11745-009-3291-9⟩
Lipids, 2009, 44 (7), pp.655-663. ⟨10.1007/s11745-009-3291-9⟩
The phospholipid fatty acid composition of the North-East Atlantic sponge Polymastia penicillus (South Brittany, France) was investigated. Sixty fatty acids (FA) were identified as methyl esters (FAME) and N-acyl pyrrolidides (NAP) by gas chromatogra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90cf922cd106c6d1c3d28d17c5ad0aa7
https://hal-nantes-universite.archives-ouvertes.fr/hal-04050369/document
https://hal-nantes-universite.archives-ouvertes.fr/hal-04050369/document
Autor:
Jean-Yves Petit, Johan Evano, Guillaume Le Baut, Nicole Grimaud, Alexandra Dassonville, Anne Breteche, Muriel Duflos
Publikováno v:
ChemInform. 36
The authors have described the synthetic way to new N-pyridinyl(methyl)indolylpropanamides acting as non acidic NSAIDs. Pharmacomodulation was carried out at N-1 and C-5 of the indole ring and at the level of the propanamide chain. N-(pyridin-3-ylmet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f00503725c1cb2401462eb757fd2eeaa
https://doi.org/10.1002/chin.200510243
https://doi.org/10.1002/chin.200510243