Bureau R - Search Results

1

The Pharmacophore Network: A Computational Method for Exploring Structure-Activity Relationships from a Large Chemical Data Set.

Métivier JP, Cuissart B, Bureau R, Lepailleur A. Métivier JP, et al. Among authors: bureau r. J Med Chem. 2018 Apr 26;61(8):3551-3564. doi: 10.1021/acs.jmedchem.7b01890. Epub 2018 Apr 18. J Med Chem. 2018. PMID: 29648816

2

Design and synthesis of a new type of non steroidal human aromatase inhibitors.

Sonnet P, Guillon J, Enguehard C, Dallemagne P, Bureau R, Rault S Auvray P, Moslemi S, Sourdiane P, Galopin S, Séralini GE. Sonnet P, et al. Among authors: bureau r. Bioorg Med Chem Lett. 1998 May 5;8(9):1041-4. doi: 10.1016/s0960-894x(98)00157-7. Bioorg Med Chem Lett. 1998. PMID: 9871704

3

New aromatase inhibitors. Synthesis and biological activity of aryl-substituted pyrrolizine and indolizine derivatives.

Sonnet P, Dallemagne P, Guillon J, Enguehard C, Stiebing S, Tanguy J, Bureau R, Rault S, Auvray P, Moslemi S, Sourdaine P, Séralini GE. Sonnet P, et al. Among authors: bureau r. Bioorg Med Chem. 2000 May;8(5):945-55. doi: 10.1016/s0968-0896(00)00024-9. Bioorg Med Chem. 2000. PMID: 10882007

4

First tricyclic oximino derivatives as 5-HT3 ligands.

Baglin I, Daveu C, Lancelot JC, Bureau R, Dauphin F, Pfeiffer B, Renard P, Delagrange P, Rault S. Baglin I, et al. Among authors: bureau r. Bioorg Med Chem Lett. 2001 Feb 26;11(4):453-7. doi: 10.1016/s0960-894x(00)00691-0. Bioorg Med Chem Lett. 2001. PMID: 11229746

5

The maximum common substructure as a molecular depiction in a supervised classification context: experiments in quantitative structure/biodegradability relationships.

Cuissart B, Touffet F, Crémilleux B, Bureau R, Rault S. Cuissart B, et al. Among authors: bureau r. J Chem Inf Comput Sci. 2002 Sep-Oct;42(5):1043-52. doi: 10.1021/ci020017w. J Chem Inf Comput Sci. 2002. PMID: 12376991

6

Synthesis and biological evaluation of five-membered heterocycles fused to cyclopenta[c]thiophene as new antitumor agents.

Dallemagne P, Khanh LP, Alsaïdi A, Varlet I, Collot V, Paillet M, Bureau R, Rault S. Dallemagne P, et al. Among authors: bureau r. Bioorg Med Chem. 2003 Apr 3;11(7):1161-7. doi: 10.1016/s0968-0896(02)00654-5. Bioorg Med Chem. 2003. PMID: 12628643

7

Molecular design based on 3D pharmacophores. Applications to 5-HT7 receptors.

Lepailleur A, Bureau R, Lemaître S, Dauphin F, Lancelot JC, Contesse V, Lenglet S, Delarue C, Vaudry H, Rault S. Lepailleur A, et al. Among authors: bureau r. J Chem Inf Comput Sci. 2004 May-Jun;44(3):1148-52. doi: 10.1021/ci030036l. J Chem Inf Comput Sci. 2004. PMID: 15154784

8

Synthesis and biological evaluation of thienopyrrolizines, a new family of CDK/GSK-3 inhibitors.

Rochais C, Lescot E, Lisowski V, Lepailleur A, Santos JS, Bureau R, Dallemagne P, Meijer L, Rault S. Rochais C, et al. Among authors: bureau r. J Enzyme Inhib Med Chem. 2004 Dec;19(6):585-93. doi: 10.1080/14756360400004565. J Enzyme Inhib Med Chem. 2004. PMID: 15662962

9

Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands.

Paillet-Loilier M, Fabis F, Lepailleur A, Bureau R, Butt-Gueulle S, Dauphin F, Delarue C, Vaudry H, Rault S. Paillet-Loilier M, et al. Among authors: bureau r. Bioorg Med Chem Lett. 2005 Aug 15;15(16):3753-7. doi: 10.1016/j.bmcl.2005.05.059. Bioorg Med Chem Lett. 2005. PMID: 16002287

10

Molecular modeling studies focused on 5-HT7 versus 5-HT1A selectivity. Discovery of novel phenylpyrrole derivatives with high affinity for 5-HT7 receptors.

Lepailleur A, Bureau R, Paillet-Loilier M, Fabis F, Saettel N, Lemaître S, Dauphin F, Lesnard A, Lancelot JC, Rault S. Lepailleur A, et al. Among authors: bureau r. J Chem Inf Model. 2005 Jul-Aug;45(4):1075-81. doi: 10.1021/ci050045p. J Chem Inf Model. 2005. PMID: 16045303

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