Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Loïc P. Chêne"'
Autor:
Albertus Viljoen, Yann Guérardel, Alexandre Mery, Maju Joe, Laurent Kremer, Sydney A. Villaume, Emeline Fabre, Christophe Mariller, Kaoru Takegawa, Stéphane P. Vincent, Lin Shen, Todd L. Lowary, Iman Halloum, Loïc P. Chêne
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2020, pp.jbc.RA119.011817. ⟨10.1074/jbc.RA119.011817⟩
Journal of Biological Chemistry, 2020, pp.jbc.RA119.011817. ⟨10.1074/jbc.RA119.011817⟩
J Biol Chem
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2020, pp.jbc.RA119.011817. ⟨10.1074/jbc.RA119.011817⟩
Journal of Biological Chemistry, 2020, pp.jbc.RA119.011817. ⟨10.1074/jbc.RA119.011817⟩
J Biol Chem
International audience; Despite the impressive progress made over the past 20 years in our understanding of mycolylarabinogalactan-peptidoglycan (mAGP) biogenesis, the mechanisms by which the tubercle bacillus Mycobacterium tuberculosis adapts its ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7361d37d2cf244f15dd89992dd74da90
https://researchportal.unamur.be/en/publications/96382eac-e4aa-4c2f-bf9c-198dca7ca6f5
https://researchportal.unamur.be/en/publications/96382eac-e4aa-4c2f-bf9c-198dca7ca6f5
Autor:
Stéphane P. Vincent, Albertus Viljoen, Laurent Kremer, Bastien Champciaux, Clément Raynaud, Emilie Thiery, Loïc P. Chêne, Jérôme Thibonnet
Publikováno v:
Champciaux, B, Raynaud, C, Viljoen, A, Chene, L, Thibonnet, J, Vincent, S P, Kremer, L & Thiery, E 2021, ' Synthesis and biological evaluation of 3,4-dihydro-1H-[1,4] oxazepino [6,5,4-hi] indol-1-ones and 4,6-dihydrooxepino [5,4,3-cd] indol-1(3H)-ones as Mycobacterium tuberculosis inhibitors ', Bioorganic and Medicinal Chemistry, vol. 43, 116248 . https://doi.org/10.1016/j.bmc.2021.116248
This study focuses on the synthesis of 1,7- and 3,4-indole-fused lactones via a simple and efficient reaction sequence. The functionalization of these “oxazepino-indole” and “oxepino-indole” tricycles is carried out by palladium catalysed C[s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35192006715ea84f52a3107243025c7c
https://pure.unamur.be/ws/files/68806981/1_s2.0_S096808962100256X_main.pdf
https://pure.unamur.be/ws/files/68806981/1_s2.0_S096808962100256X_main.pdf
Autor:
Kuo-Shyan Lin, Sergii Afonin, Justin J. Bailey, Pablo Barrio, Francois Benard, Vadim Bernard-Gauthier, Thierry Billard, Silvestre Buscemi, Fabien Caillé, Loïc P. Chêne, Julien A. Delbrouck, Kevin D. Dykstra, Myriem El Qacemi, Lori Fitz, Santos Fustero, Jéôme Graton, Oliver Gutbrod, Tadashi Honda, Luke Hunter, Naoko Ichiishi, Peter Jeschke, Klaus Jurkschat, Igor V. Komarov, Olga Koshkina, Shane W. Krska, Bertrand Kuhnast, Jean-Yves Le Questel, Frederic R. Leroux, François Liger, Bruno Linclau, Peter Maienfisch, Flora Mansour, Klaus Müller, Cormac D. Murphy, Iwao Ojima, Andrea Pace, William Palmer-Brown, Antonio Palumbo Piccionello, David M. Perrin, Fabrizio Pertusati, Ivana Pibiri, Elisa Pileggi, Laura Quinn, Stefano Rendine, Paul F. Richardson, Mélanie Roche, Raquel Román, Marta Saccomanno, Ralf Schirrmacher, Esther Schirrmacher, Daniel M. Sedgwick, Michaela Serpi, Simon Specklin, Mangala Srinivas, Xander Staal, Andrés A. Trabanco, Anne S. Ulrich, Mathieu Verdurand, Stéphane P. Vincent, Carmen Wängler, Björn Wängler, Li Xing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68e6cf90fd569787b54636f8c72764fe
https://doi.org/10.1016/b978-0-12-812733-9.01002-3
https://doi.org/10.1016/b978-0-12-812733-9.01002-3
Fluorinated carbohydrates play a major role in PET-Scan imaging and as diagnostic tools. They have also been instrumental tools to decipher the mechanism of key glycosyl-processing enzymes. The emergence of bacterial resistance to antibiotics has for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50788d5d6876e45a591424d623a2e9e6
https://doi.org/10.1016/b978-0-12-812733-9.00006-4
https://doi.org/10.1016/b978-0-12-812733-9.00006-4