Renard P - Search Results

1

3-amino-3,4-dihydro-2H-1-benzopyran derivatives as 5-HT1A receptor ligands and potential anxiolytic agents. 2. Synthesis and quantitative structure-activity relationship studies of spiro[pyrrolidine- and piperidine-2,3'(2'H)-benzopyrans].

Comoy C, Marot C, Podona T, Baudin ML, Morin-Allory L, Guillaumet G, Pfeiffer B, Caignard DH, Renard P, Rettori MC, Adam G, Guardiola-Lemaitre B. Comoy C, et al. Among authors: renard p. J Med Chem. 1996 Oct 11;39(21):4285-98. doi: 10.1021/jm950861w. J Med Chem. 1996. PMID: 8863806

2

Synthesis and biological evaluation of new 2-(4,5-dihydro-1H-imidazol-2-yl)-3,4-dihydro-2H-1,4-benzoxazine derivatives.

Touzeau F, Arrault A, Guillaumet G, Scalbert E, Pfeiffer B, Rettori MC, Renard P, Mérour JY. Touzeau F, et al. Among authors: renard p. J Med Chem. 2003 May 8;46(10):1962-79. doi: 10.1021/jm021050c. J Med Chem. 2003. PMID: 12723959

3

Studies towards the conception of new selective PPARbeta/delta ligands.

Basséne CE, Suzenet F, Hennuyer N, Staels B, Caignard DH, Dacquet C, Renard P, Guillaumet G. Basséne CE, et al. Among authors: renard p. Bioorg Med Chem Lett. 2006 Sep 1;16(17):4528-32. doi: 10.1016/j.bmcl.2006.06.028. Epub 2006 Jun 23. Bioorg Med Chem Lett. 2006. PMID: 16797985

4

N-substituted aminohydroxypyridines as potential non-opioid analgesic agents.

Viaud MC, Jamoneau P, Bizot-Espiard JG, Pfeiffer B, Renard P, Caignard DH, Adam G, Guillaumet G. Viaud MC, et al. Among authors: renard p. Bioorg Med Chem. 1995 Jul;3(7):929-37. doi: 10.1016/0968-0896(95)00080-z. Bioorg Med Chem. 1995. PMID: 7582970

5

N-substituted oxazolo[5,4-b]pyridin-2(1H)-ones: a new class of non-opiate antinociceptive agents.

Viaud MC, Jamoneau P, Flouzat C, Bizot-Espiard JG, Pfeiffer B, Renard P, Caignard DH, Adam G, Guillaumet G. Viaud MC, et al. Among authors: renard p. J Med Chem. 1995 Apr 14;38(8):1278-86. doi: 10.1021/jm00008a006. J Med Chem. 1995. PMID: 7731014

6

3,4-Dihydro-3-amino-2H-1-benzopyran derivatives as 5-HT1A receptor ligands and potential anxiolytic agents. 1. Synthesis and structure--activity relationship studies.

Podona T, Guardiola-Lemaître B, Caignard DH, Adam G, Pfeiffer B, Renard P, Guillaumet G. Podona T, et al. Among authors: renard p. J Med Chem. 1994 Jun 10;37(12):1779-93. doi: 10.1021/jm00038a007. J Med Chem. 1994. PMID: 7912735

7

Synthesis and structure-activity relationships of novel naphthalenic and bioisosteric related amidic derivatives as melatonin receptor ligands.

Depreux P, Lesieur D, Mansour HA, Morgan P, Howell HE, Renard P, Caignard DH, Pfeiffer B, Delagrange P, Guardiola B, et al. Depreux P, et al. Among authors: renard p. J Med Chem. 1994 Sep 30;37(20):3231-9. doi: 10.1021/jm00046a006. J Med Chem. 1994. PMID: 7932550

8

Novel selective and partial agonists of 5-HT3 receptors. Part 1. Synthesis and biological evaluation of piperazinopyrrolothienopyrazines.

Rault S, Lancelot JC, Prunier H, Robba M, Renard P, Delagrange P, Pfeiffer B, Caignard DH, Guardiola-Lemaitre B, Hamon M. Rault S, et al. Among authors: renard p. J Med Chem. 1996 May 10;39(10):2068-80. doi: 10.1021/jm950543x. J Med Chem. 1996. PMID: 8642566

9

Novel indole-2-carboxamide and cycloalkeno[1,2-b]indole derivatives. Structure-activity relationships for high inhibition of human LDL peroxidation.

Kuehm-Caubere C, Caubere P, Jamart-Gregoire B, Negre-Salvayre A, Bonnefont-Rousselot D, Bizot-Espiard JG, Pfeiffer B, Caignard DH, Guardiola-Lemaitre B, Renard P. Kuehm-Caubere C, et al. Among authors: renard p. J Med Chem. 1997 Apr 11;40(8):1201-10. doi: 10.1021/jm960542k. J Med Chem. 1997. PMID: 9111294

10

Novel and selective partial agonists of 5-HT3 receptors. 2. Synthesis and biological evaluation of piperazinopyridopyrrolopyrazines, piperazinopyrroloquinoxalines, and piperazinopyridopyrroloquinoxalines.

Prunier H, Rault S, Lancelot JC, Robba M, Renard P, Delagrange P, Pfeiffer B, Caignard DH, Misslin R, Guardiola-Lemaitre B, Hamon M. Prunier H, et al. Among authors: renard p. J Med Chem. 1997 Jun 6;40(12):1808-19. doi: 10.1021/jm960501o. J Med Chem. 1997. PMID: 9191957

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