Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Vincent Moret"'
Autor:
Vincent Moret
Every chess player needs to decide which openings he or she is going to play. But where do you start? The risk of drowning in the turbulent sea of chess opening theory is only too real for beginning amateurs.Often your goals and ambitions will be mis
Autor:
Vincent Moret
Every chess player needs to decide which openings he is going to play. But where do you start? The risk of drowning in the turbulent sea of opening theory is only too real for beginning amateurs.Often your goals and ambitions will be misguided. Tryin
Autor:
Amandine Rolland, C. Weck, C. Garino, Younes Laras, Jean-Louis Kraus, Vincent Moret, Jean Dessolin
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 24:181-187
Synthesis and enzymatic evaluation of new series of N(4)-substituted piperazine naphthamide derivatives as BACE-1 inhibitors for the treatment of Alzheimer's disease are reported.
Autor:
Jean-Chrétien Norreel, Jean-Louis Kraus, Isabelle Boquet, Amandine Rolland, Vincent Moret, Younes Laras
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2008, 18, pp.169-174
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2008, 18, pp.169-174
Bioorganic and Medicinal Chemistry Letters, 2008, 18, pp.169-174
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2008, 18, pp.169-174
Using SVZ (subventricular zone) tissue explants from one-day-old mice, we investigated the activity of new amino aromatic disulfide analogues and polyazamacrocycles on the migration of SVZ cells (neuroblasts). We found that among the tested analogues
Autor:
Jean-Chrétien Norreel, Jean-Louis Kraus, Gilles Quéléver, Younes Laras, Bernard Mallet, Amandine Rolland, Cédrik Garino, Vincent Moret, Nicolas Pietrancosta
Publikováno v:
HAL
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2006, 16, pp.3298-3301
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16, pp.3298-3301
Bioorganic and Medicinal Chemistry Letters, 2006, 16 (12), pp.3298-3301. ⟨10.1016/j.bmcl.2006.03.026⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16 (12), pp.3298-3301. ⟨10.1016/j.bmcl.2006.03.026⟩
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2006, 16, pp.3298-3301
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16, pp.3298-3301
Bioorganic and Medicinal Chemistry Letters, 2006, 16 (12), pp.3298-3301. ⟨10.1016/j.bmcl.2006.03.026⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16 (12), pp.3298-3301. ⟨10.1016/j.bmcl.2006.03.026⟩
Dysfunction of copper metabolism leading to its excess or deficiency results in severe ailments. Recently, neurodegenerative disorders such as Alzheimer’s disease have been associated with copper metabolism. Compounds having the ability to reduce c
Autor:
Magali Barthelemy-Requin, Sabine Depauw, Delphine Lamoral-Theys, Jacques Dubois, Sébastien Madonna, Gaëlle Lenglet, Thierry Cresteil, Marie-Hélène David-Cordonnier, Christophe Beclin, Jean-Louis Kraus, Valérie Monnier, Robert Kiss, Geneviève Aubert, Younes Laras, Aline Marcowycz, Vincent Moret
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2010, 45 (2), pp.623-638. 〈10.1016/j.ejmech.2009.11.006〉
European Journal of Medicinal Chemistry, 2010, 45 (2), pp.623-638. ⟨10.1016/j.ejmech.2009.11.006⟩
European Journal of Medicinal Chemistry, Elsevier, 2010, 45 (2), pp.623-638. ⟨10.1016/j.ejmech.2009.11.006⟩
European Journal of Medicinal Chemistry, Elsevier, 2010, 45 (2), pp.623-38. ⟨10.1016/j.ejmech.2009.11.006⟩
European Journal of Medicinal Chemistry, Elsevier, 2010, 45 (2), pp.623-638. 〈10.1016/j.ejmech.2009.11.006〉
European Journal of Medicinal Chemistry, 2010, 45 (2), pp.623-638. ⟨10.1016/j.ejmech.2009.11.006⟩
European Journal of Medicinal Chemistry, Elsevier, 2010, 45 (2), pp.623-638. ⟨10.1016/j.ejmech.2009.11.006⟩
European Journal of Medicinal Chemistry, Elsevier, 2010, 45 (2), pp.623-38. ⟨10.1016/j.ejmech.2009.11.006⟩
International audience; A series of twenty six 8-hydroxyquinoline substituted amines, structurally related to compounds 2 and 3, were synthesized to evaluate the effects of structural changes on antitumor activity and understand their mechanism of ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b58b3dd6308b3f3e7310ac0534516a3
https://hal.archives-ouvertes.fr/hal-00563139
https://hal.archives-ouvertes.fr/hal-00563139
Autor:
Vincent Peyrot, Thierry Cresteil, Diane Allegro, Eleonora Petrucci, Ugo Testa, Francesca De Angelis, Younes Laras, Evelina Gatti, Vincent Moret, Dou Q. Ping, Jean -Louis Kraus, Luca Pasquini, Chen Di, Christophe Beclin, Magali Barthelemy-Requin, Philippe Pierre, Geneviève Aubert, Amandine Rolland
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2009, 44 (2), pp.558-567. ⟨10.1016/j.ejmech.2008.03.042⟩
European Journal of Medicinal Chemistry, Elsevier, 2008, 44 (2), pp.558-557. ⟨10.1016/j.ejmech.2008.03.042⟩
European Journal of Medicinal Chemistry, 2008, 44 (2), pp.558-557. ⟨10.1016/j.ejmech.2008.03.042⟩
European Journal of Medicinal Chemistry, Elsevier, 2009, 44, pp.558-567. ⟨10.1016/j.ejmech.2008.03.042⟩
European Journal of Medicinal Chemistry, Elsevier, 2009, 44 (2), pp.558-567. ⟨10.1016/j.ejmech.2008.03.042⟩
European Journal of Medicinal Chemistry, Elsevier, 2008, 44 (2), pp.558-557. ⟨10.1016/j.ejmech.2008.03.042⟩
European Journal of Medicinal Chemistry, 2008, 44 (2), pp.558-557. ⟨10.1016/j.ejmech.2008.03.042⟩
European Journal of Medicinal Chemistry, Elsevier, 2009, 44, pp.558-567. ⟨10.1016/j.ejmech.2008.03.042⟩
International audience; Bis-8-hydroxyquinoline substituted benzylamines have been synthesized and screened for their antitumor activity on KB3 cell line model. Synthesis of this series of new analogues was accomplished using a one pot specific method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8be47639b7a3a421a5a9a873716248a6
https://hal.archives-ouvertes.fr/hal-00353436
https://hal.archives-ouvertes.fr/hal-00353436
Publikováno v:
ChemInform. 38
Autor:
Vincent Moret, Jean-Louis Kraus, Amandine Rolland, Clement Weck, Younes Laras, Pascal Clayette, Sylvain Marc, Nathalie Dereudre-Bosquet, Nicolas Pietrancosta
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2006, 16 (23), pp.5988-5992. ⟨10.1016/j.bmcl.2006.08.114⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16 (23), pp.5988-5992. ⟨10.1016/j.bmcl.2006.08.114⟩
Bioorganic and Medicinal Chemistry Letters, 2006, 16 (23), pp.5988-5992. ⟨10.1016/j.bmcl.2006.08.114⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16 (23), pp.5988-5992. ⟨10.1016/j.bmcl.2006.08.114⟩
To find new derivatives that block different virus strains entry in cells bearing specific surface receptors represent an interesting challenge for medicinal chemists. Here, we report the synthesis and the anti-HIV properties of a new series of analo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab7e6d1984b491a82a679f7d4ecce0a2
https://hal.science/hal-02351693
https://hal.science/hal-02351693
Autor:
Amandine Rolland, Cédrik Garino, Vincent Moret, Younes Laras, Nicolas Pietrancosta, Jean-Louis Kraus, Gilles Quéléver
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16 (7), pp.1995-1999. ⟨10.1016/j.bmcl.2005.12.064⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16, pp.1995-1999
Bioorganic and Medicinal Chemistry Letters, 2006, 16 (7), pp.1995-1999. ⟨10.1016/j.bmcl.2005.12.064⟩
Bioorganic and Medicinal Chemistry Letters, 2006, 16, pp.1995-1999
HAL
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16 (7), pp.1995-1999. ⟨10.1016/j.bmcl.2005.12.064⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16, pp.1995-1999
Bioorganic and Medicinal Chemistry Letters, 2006, 16 (7), pp.1995-1999. ⟨10.1016/j.bmcl.2005.12.064⟩
Bioorganic and Medicinal Chemistry Letters, 2006, 16, pp.1995-1999
HAL
The protease beta-secretase plays a central role in the synthesis of pathogenic amyloid-beta in Alzheimer's disease. Here, we report a new series of analogues based on the phenyl-piperazine scaffold coupled to various heterocyclic moieties, which dem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3746b6d91ac358393aaf00e50be24f14
https://hal.archives-ouvertes.fr/hal-02351707
https://hal.archives-ouvertes.fr/hal-02351707