Bourguignon JJ - Search Results

1

Inhibition of platelet function by administration of MRS2179, a P2Y1 receptor antagonist.

Baurand A, Raboisson P, Freund M, Léon C, Cazenave JP, Bourguignon JJ, Gachet C. Baurand A, et al. Among authors: bourguignon jj. Eur J Pharmacol. 2001 Feb 2;412(3):213-21. doi: 10.1016/s0014-2999(01)00733-6. Eur J Pharmacol. 2001. PMID: 11166284

2

Novel antagonists acting at the P2Y(1) purinergic receptor: synthesis and conformational analysis using potentiometric and nuclear magnetic resonance titration techniques.

Raboisson P, Baurand A, Cazenave JP, Gachet C, Retat M, Spiess B, Bourguignon JJ. Raboisson P, et al. Among authors: bourguignon jj. J Med Chem. 2002 Feb 14;45(4):962-72. doi: 10.1021/jm0104062. J Med Chem. 2002. PMID: 11831909

3

A general approach toward the synthesis of C-nucleoside pyrazolo[1,5-a]-1,3,5-triazines and their 3',5'-bisphosphate C-nucleotide analogues as the first reported in vivo stable P2Y(1)-receptor antagonists.

Raboisson P, Baurand A, Cazenave JP, Gachet C, Schultz D, Spiess B, Bourguignon JJ. Raboisson P, et al. Among authors: bourguignon jj. J Org Chem. 2002 Nov 15;67(23):8063-71. doi: 10.1021/jo026268l. J Org Chem. 2002. PMID: 12423133

4

Synthesis and biological activity of 2-alkylated deoxyadenosine bisphosphate derivatives as P2Y(1) receptor antagonists.

Mathieu R, Baurand A, Schmitt M, Gachet C, Bourguignon JJ. Mathieu R, et al. Among authors: bourguignon jj. Bioorg Med Chem. 2004 Apr 1;12(7):1769-79. doi: 10.1016/j.bmc.2003.12.041. Bioorg Med Chem. 2004. PMID: 15028267

5

9-Benzyladenines: potent and selective cAMP phosphodiesterase inhibitors.

Bourguignon JJ, Désaubry L, Raboisson P, Wermuth CG, Lugnier C. Bourguignon JJ, et al. J Med Chem. 1997 Jun 6;40(12):1768-70. doi: 10.1021/jm960827x. J Med Chem. 1997. PMID: 9191951 No abstract available.

6

Anti-TNF-alpha properties of new 9-benzyladenine derivatives with selective phosphodiesterase-4- inhibiting properties.

Reimund JM, Raboisson P, Pinna G, Lugnier C, Bourguignon JJ, Muller CD. Reimund JM, et al. Among authors: bourguignon jj. Biochem Biophys Res Commun. 2001 Oct 26;288(2):427-34. doi: 10.1006/bbrc.2001.5786. Biochem Biophys Res Commun. 2001. PMID: 11606060

7

Design, synthesis and structure-activity relationships of a series of 9-substituted adenine derivatives as selective phosphodiesterase type-4 inhibitors.

Raboisson P, Lugnier C, Muller C, Reimund JM, Schultz D, Pinna G, Le Bec A, Basaran H, Desaubry L, Gaudiot F, Seloum M, Bourguignon JJ. Raboisson P, et al. Among authors: bourguignon jj. Eur J Med Chem. 2003 Feb;38(2):199-214. doi: 10.1016/s0223-5234(02)01446-0. Eur J Med Chem. 2003. PMID: 12620664

8

Cyclic nucleotide phosphodiesterase type 4 inhibitors: evaluation of pyrazolo[1,5-a]-1,3,5-triazine ring system as an adenine bioisostere.

Raboisson P, Schultz D, Muller C, Reimund JM, Pinna G, Mathieu R, Bernard P, Do QT, Desjarlais RL, Justiano H, Lugnier C, Bourguignon JJ. Raboisson P, et al. Among authors: bourguignon jj. Eur J Med Chem. 2008 Apr;43(4):816-29. doi: 10.1016/j.ejmech.2007.05.016. Epub 2007 Jun 8. Eur J Med Chem. 2008. PMID: 17640774

9

Anti-sedative and anti-cataleptic properties of NCS-382, a gamma-hydroxybutyrate receptor antagonist.

Schmidt C, Gobaille S, Hechler V, Schmitt M, Bourguignon JJ, Maitre M. Schmidt C, et al. Among authors: bourguignon jj. Eur J Pharmacol. 1991 Oct 22;203(3):393-7. doi: 10.1016/0014-2999(91)90896-x. Eur J Pharmacol. 1991. PMID: 1773824

10

A specific gamma-hydroxybutyrate receptor ligand possesses both antagonistic and anticonvulsant properties.

Maitre M, Hechler V, Vayer P, Gobaille S, Cash CD, Schmitt M, Bourguignon JJ. Maitre M, et al. Among authors: bourguignon jj. J Pharmacol Exp Ther. 1990 Nov;255(2):657-63. J Pharmacol Exp Ther. 1990. PMID: 2173754

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