Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nadine Payrot"'
Autor:
Ndeye Mathy Kebe, Krishnananda Samanta, Priyanka Singh, Joséphine Lai-Kee-Him, Viviana Apicella, Nadine Payrot, Noémie Lauraire, Baptiste Legrand, Vincent Lisowski, Diane-Ethna Mbang-Benet, Michel Pages, Patrick Bastien, Andrey V. Kajava, Patrick Bron, Jean-François Hernandez, Olivier Coux
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 5, p 1021 (2019)
HslVU is an ATP-dependent proteolytic complex present in certain bacteria and in the mitochondrion of some primordial eukaryotes, including deadly parasites such as Leishmania. It is formed by the dodecameric protease HslV and the hexameric ATPase Hs
Externí odkaz:
https://doaj.org/article/e99f6b0b89734195bb6d28a240030dcd
Autor:
Bruno Canard, Loic Roux, Karine Alvarez, Clément Weck, Fabien Zoulim, Nadine Payrot, Jan Balzarini, Maëlenn Fournier, Stéphane Priet
Publikováno v:
European Journal of Medicinal Chemistry. 63:869-881
9-[2-(Thiophosphonomethoxy)ethyl]adenine [S-PMEA, 8] and (R)-9-[2-(Thiophosphonomethoxy)propyl]adenine [S-PMPA, 9] are acyclic nucleoside thiophosphonates we described recently that display the same antiviral spectrum (DNA viruses) as approved and po
Autor:
Jean Martinez, Michel Khrestchatisky, Vincent Lisowski, Marion David, Franck Debarbieux, Patrick Vlieghe, Karima Abouzid, Aude Faucon, Nadine Payrot, Geneviève Rougon, Guillaume Jacquot, Nicolas Floquet, Jean-Daniel Malcor
Publikováno v:
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2012, 55 (5), pp.2227-41. ⟨10.1021/jm2014919⟩
Journal of Medicinal Chemistry, American Chemical Society, 2012, 55 (5), pp.2227-41. 〈10.1021/jm2014919〉
Journal of Medicinal Chemistry, 2012, 55 (5), pp.2227-41. ⟨10.1021/jm2014919⟩
Journal of Medicinal Chemistry, American Chemical Society, 2012, 55 (5), pp.2227-41. ⟨10.1021/jm2014919⟩
Journal of Medicinal Chemistry, American Chemical Society, 2012, 55 (5), pp.2227-41. 〈10.1021/jm2014919〉
Journal of Medicinal Chemistry, 2012, 55 (5), pp.2227-41. ⟨10.1021/jm2014919⟩
International audience; Drug delivery to the central nervous system is hindered by the presence of physiological barriers such as the blood-brain barrier. To accomplish the task of nutrient transport, the brain endothelium is endowed with various tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::611f4970f78d8beffc7c8e16e685d80d
https://hal.archives-ouvertes.fr/hal-00839126
https://hal.archives-ouvertes.fr/hal-00839126
Autor:
Bruno Canard, Johan Neyts, Céline Durafour, Loic Roux, Stéphane Priet, Nadine Payrot, Karine Barral, Fabien Zoulim, Karine Alvarez, Clément Weck, Jan Balzarini
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2011, 46 (9), pp.4281-4288. ⟨10.1016/j.ejmech.2011.06.034⟩
European Journal of Medicinal Chemistry, Elsevier, 2011, 46 (9), pp.4281-8. ⟨10.1016/j.ejmech.2011.06.034⟩
European Journal of Medicinal Chemistry, 2011, 46 (9), pp.4281-4288. ⟨10.1016/j.ejmech.2011.06.034⟩
European Journal of Medicinal Chemistry, Elsevier, 2011, 46 (9), pp.4281-4288. ⟨10.1016/j.ejmech.2011.06.034⟩
European Journal of Medicinal Chemistry, Elsevier, 2011, 46 (9), pp.4281-8. ⟨10.1016/j.ejmech.2011.06.034⟩
European Journal of Medicinal Chemistry, 2011, 46 (9), pp.4281-4288. ⟨10.1016/j.ejmech.2011.06.034⟩
9-[2-(Thiophosphonomethoxy)ethyl]adenine 3 and (R)-9-[2-(Thiophosphonomethoxy)propyl]adenine 4 were synthesized as the first thiophosphonate nucleosides bearing a sulfur atom at the α-position of the acyclic nucleoside phosphonates PMEA and PMPA. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422ac416b607150ab35968d5e1b59a1d
https://hal-amu.archives-ouvertes.fr/hal-02061721
https://hal-amu.archives-ouvertes.fr/hal-02061721