Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Sandrine, Grosse"'
Autor:
Xiaodi Yu, Pravien Abeywickrema, Brecht Bonneux, Ishani Behera, Brandon Anson, Edgar Jacoby, Amy Fung, Suraj Adhikary, Anusarka Bhaumik, Rodrigo J. Carbajo, Suzanne De Bruyn, Robyn Miller, Aaron Patrick, Quyen Pham, Madison Piassek, Nick Verheyen, Afzaal Shareef, Priscila Sutto-Ortiz, Nina Ysebaert, Herman Van Vlijmen, Tim H. M. Jonckers, Florence Herschke, Jason S. McLellan, Etienne Decroly, Rachel Fearns, Sandrine Grosse, Dirk Roymans, Sujata Sharma, Peter Rigaux, Zhinan Jin
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-12 (2023)
Abstract The respiratory syncytial virus polymerase complex, consisting of the polymerase (L) and phosphoprotein (P), catalyzes nucleotide polymerization, cap addition, and cap methylation via the RNA dependent RNA polymerase, capping, and Methyltran
Externí odkaz:
https://doaj.org/article/155faab50b5b48fe954bff5b07e1b8ac
Autor:
Sandrine Grosse, Abdellah Tahri, Pierre Raboisson, Yannis Houpis, Bart Stoops, Edgar Jacoby, Jean-Marc Neefs, Marnix Van Loock, Olivia Goethals, Peggy Geluykens, Jean-François Bonfanti, Tim H. M. Jonckers
Publikováno v:
ACS Medicinal Chemistry Letters. 13:1879-1884
In continuation of our efforts of finding novel nucleoside inhibitors for the treatment of viral diseases, we initiated a discovery research program aimed at identifying novel nucleos(t)ide inhibitors for emerging diseases like Dengue and Chikungunya
Autor:
Pierre Sierocki, Krystal Gaillard, Ruben Arturo Arellano Reyes, Chloé Donnart, Emilie Lambert, Sandrine Grosse, Laurence Arzel, Arnaud Tessier, Jerome Guillemont, Monique Mathé-Allainmat, Jacques Lebreton
Publikováno v:
Organic & Biomolecular Chemistry. 20:2715-2728
We report the synthesis of C-nucleosides with a quaternary carbon at the anomeric position tethered to a 4-substituted 1,2,3-triazole ring and a cyano group, which were developed as potential antiviral agents.
Autor:
Lionel Tarrago, Sandrine Grosse, David Lemaire, Laetitia Faure, Mathilde Tribout, Marina I. Siponen, Mila Kojadinovic-Sirinelli, David Pignol, Pascal Arnoux, Monique Sabaty
Publikováno v:
Antioxidants, Vol 9, Iss 7, p 616 (2020)
In proteins, methionine (Met) can be oxidized into Met sulfoxide (MetO). The ubiquitous methionine sulfoxide reductases (Msr) A and B are thiol-oxidoreductases reducing MetO. Reversible Met oxidation has a wide range of consequences, from protection
Externí odkaz:
https://doaj.org/article/899b7eb4284347f69ea41f438d42ea3a
Autor:
Pierre, Sierocki, Krystal, Gaillard, Ruben Arturo, Arellano Reyes, Chloé, Donnart, Emilie, Lambert, Sandrine, Grosse, Laurence, Arzel, Arnaud, Tessier, Jerome, Guillemont, Monique, Mathé-Allainmat, Jacques, Lebreton
Publikováno v:
Organicbiomolecular chemistry. 20(13)
A linear sequence to access a novel series of
Autor:
Lionel Tarrago, Lise Molinelli, David Lemaire, Mathilde Tribout, Sandrine Grosse, May Belghazi, Thierry Tron, David Pignol, Monique Sabaty, Pascal Arnoux
Publikováno v:
Free Radical Biology and Medicine. 189:19
Autor:
Bruno Guigliarelli, David Pignol, Kamal Zeamari, Guillaume Gerbaud, Florence Chaspoul, Pascal Arnoux, Bénédicte Burlat, Monique Sabaty, Sandrine Grosse, Vincent Fourmond, Frédéric Biaso
Publikováno v:
Biochimica biophysica acta (BBA)-Bioenergetics
Biochimica biophysica acta (BBA)-Bioenergetics, Elsevier, 2019, 1860 (5), pp.402-413. ⟨10.1016/j.bbabio.2019.01.003⟩
Biochimica biophysica acta (BBA)-Bioenergetics, 2019, 1860 (5), pp.402-413. ⟨10.1016/j.bbabio.2019.01.003⟩
Biochimica biophysica acta (BBA)-Bioenergetics, Elsevier, 2019, 1860 (5), pp.402-413. ⟨10.1016/j.bbabio.2019.01.003⟩
Biochimica biophysica acta (BBA)-Bioenergetics, 2019, 1860 (5), pp.402-413. ⟨10.1016/j.bbabio.2019.01.003⟩
Molybdoenzymes are ubiquitous in living organisms and catalyze, for most of them, oxidation-reduction reactions using a large range of substrates. Periplasmic nitrate reductase (NapAB) from Rhodobacter sphaeroides catalyzes the 2-electron reduction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a315a22af5869c3c3d8d38817957028
https://hal-amu.archives-ouvertes.fr/hal-02106668
https://hal-amu.archives-ouvertes.fr/hal-02106668
Autor:
Sandrine Grosse, Guylaine Miotello, Pascal Arnoux, David Lemaire, Lionel Tarrago, Marina I. Siponen, Jean Armengaud, David Pignol, Béatrice Alonso, Monique Sabaty
Publikováno v:
Biochemical Journal
Biochemical Journal, 2018, 475 (23), pp.3779-3795. ⟨10.1042/BCJ20180706⟩
Biochemical Journal, Portland Press, 2018, 475 (23), pp.3779-3795. ⟨10.1042/BCJ20180706⟩
Biochemical Journal, 2018, 475 (23), pp.3779-3795. ⟨10.1042/BCJ20180706⟩
Biochemical Journal, Portland Press, 2018, 475 (23), pp.3779-3795. ⟨10.1042/BCJ20180706⟩
International audience; Methionine (Met) is prone to oxidation and can be converted to Met sulfoxide (MetO), which exists as $R$- and $S$-diastereomers. MetO can be reduced back to Met by the ubiquitous methionine sulfoxide reductase (Msr) enzymes. C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10d5e7bc7c5d52f229033957dc37e59e
https://cea.hal.science/cea-01936753
https://cea.hal.science/cea-01936753
Autor:
David Lemaire, Monique Sabaty, Jean Armengaud, David Pignol, Lionel Tarrago, Pascal Arnoux, Sandrine Grosse, Guylaine Miotello, Marina I. Siponen, Béatrice Alonso
SummaryMethionine (Met) is prone to oxidation and can be converted to Met sulfoxide (MetO), which exists as R- and S-diastereomers. MetO can be reduced back to Met by the ubiquitous methionine sulfoxide reductase (Msr) enzymes. Canonical MsrA and Msr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecd14b20bc25502145fe6596d0ee713f
Autor:
Christelle Pillard, Gérald Guillaumet, Philippe Bernard, Robert Kiss, Mathieu Marchivie, Stéphane Massip, Christian Jarry, Sandrine Grosse, Véronique Mathieu
Publikováno v:
European Journal of Medicinal Chemistry. 84:718-730
Synthesis and functionalization strategies of the imidazo[1,2-b]pyrazole core were developed giving a rapid access to three series of novel imidazo[1,2-b]pyrazole type derivatives: C-2/C-6/C-7 trisubstituted, C-2/C-3/C-6 tri(hetero)arylated and C-2/C