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Results: 1-25 | 26-50 | 51-65 |
Results: 51-65/65
Novel thiopyrano[3,2-b] and cycloalkeno[1,2-b]indole derivatives with highinhibitory properties in LTB4 production
Authors: Kuehm-Caubere, C Caubere, P Jamart-Gregoire, B Pfeiffer, B Guardiola-Lemaitre, P Manechez, D Renard, P
Citation: C. Kuehm-caubere et al., Novel thiopyrano[3,2-b] and cycloalkeno[1,2-b]indole derivatives with highinhibitory properties in LTB4 production, EUR J MED C, 34(1), 1999, pp. 51-61
Antagonistic effects of S 22153, a new mt1 and MT2 receptor ligand, on theneophobia-reducing properties of melatonin in BALB/c mice
Authors: Kopp, C Vogel, E Rettori, MC Delagrange, P Renard, P Lesieur, D Misslin, R
Citation: C. Kopp et al., Antagonistic effects of S 22153, a new mt1 and MT2 receptor ligand, on theneophobia-reducing properties of melatonin in BALB/c mice, PHARM BIO B, 64(1), 1999, pp. 131-136
Paul Morand's 'France-la-Doulce' (1934), or cinema according to the FrenchRight wing
Authors: Renard, P
Citation: P. Renard, Paul Morand's 'France-la-Doulce' (1934), or cinema according to the FrenchRight wing, POSITIF, (460), 1999, pp. 64-66
Isomers of substituted 3-benzo[b]furyl and 3-thienylaminobutyric acids as potent ligands of the GABA-B receptor: synthesis and preparative liquid chromatographic separation
Authors: Ansar, M Ebrik, S Mouhoub, R Vaccher, C Vaccher, MP Flouquet, N Bakkas, S Taoufik, J Debaert, M Caignard, DH Renard, P Berthelot, P
Citation: M. Ansar et al., Isomers of substituted 3-benzo[b]furyl and 3-thienylaminobutyric acids as potent ligands of the GABA-B receptor: synthesis and preparative liquid chromatographic separation, THERAPIE, 54(5), 1999, pp. 651-658
Design and synthesis of imidazoline derivatives active on glucose homeostasis in a rat model of type II diabetes. 2. Syntheses and biological activities of 1,4-dialkyl-,1,4-dibenzyl, and 1-benzyl-4-alkyl-2-(4 ',5 '-dihydro-1' H-imidazol-2 '-yl)piperazines and isosteric analogues of imidazoline
Authors: Le Bihan, G Rondu, F Pele-Tounian, A Wang, X Lidy, S Touboul, E Lamouri, A Dive, G Huet, J Pfeiffer, B Renard, P Guardiola-Lemaitre, B Manechez, D Penicaud, L Ktorza, A Godfroid, JJ
Citation: G. Le Bihan et al., Design and synthesis of imidazoline derivatives active on glucose homeostasis in a rat model of type II diabetes. 2. Syntheses and biological activities of 1,4-dialkyl-,1,4-dibenzyl, and 1-benzyl-4-alkyl-2-(4 ',5 '-dihydro-1' H-imidazol-2 '-yl)piperazines and isosteric analogues of imidazoline, J MED CHEM, 42(9), 1999, pp. 1587-1603
Melatonergic properties of the (+)- and (-)-enantiomers of N-(4-methoxy-2,3-dihydro-1H-phenalen-2-yl) amide derivatives
Authors: Jellimann, C Mathe-Allainmat, M Andrieux, J Renard, P Delagrange, P Langlois, M
Citation: C. Jellimann et al., Melatonergic properties of the (+)- and (-)-enantiomers of N-(4-methoxy-2,3-dihydro-1H-phenalen-2-yl) amide derivatives, J MED CHEM, 42(6), 1999, pp. 1100-1105
Synthesis and structure-activity relationships of new 1,3-disubstituted cyclohexanes as structurally rigid leukotriene B-4 receptor antagonists
Authors: Poudrel, JM Hullot, P Vidal, JP Girard, JP Rossi, JC Muller, A Bonne, C Bezuglov, V Serkov, I Renard, P Pfeiffer, B
Citation: Jm. Poudrel et al., Synthesis and structure-activity relationships of new 1,3-disubstituted cyclohexanes as structurally rigid leukotriene B-4 receptor antagonists, J MED CHEM, 42(26), 1999, pp. 5289-5310
Inducible degradation of I kappa B alpha by the proteasome requires interaction with the F-box protein h-beta TrCP
Authors: Kroll, M Margottin, F Kohl, A Renard, P Durand, H Concordet, JP Bachelerie, F Arenzana-Seisdedos, F Benarous, R
Citation: M. Kroll et al., Inducible degradation of I kappa B alpha by the proteasome requires interaction with the F-box protein h-beta TrCP, J BIOL CHEM, 274(12), 1999, pp. 7941-7945
A reader sends in his great-grandfather's permanent pass from 1915
Authors: Renard, P
Citation: P. Renard, A reader sends in his great-grandfather's permanent pass from 1915, HISTORIA, (636), 1999, pp. 6-6
Effect of the new imidazoline derivative S-22068 (PMS 847) on insulin secretion in vitro and glucose turnover in vivo in rats
Authors: Pele-Tounian, A Chan, SLF Rondu, F Le Bihan, G Giroix, MH Lamouri, A Touboul, E Pfeiffer, B Manechez, D Renard, P Guardiola-Lemaitre, B Godfroid, JJ Penicaud, L Morgan, NG Ktorza, A
Citation: A. Pele-tounian et al., Effect of the new imidazoline derivative S-22068 (PMS 847) on insulin secretion in vitro and glucose turnover in vivo in rats, EUR J PHARM, 377(1), 1999, pp. 81-87
A single oral dose of S 22153, a melatonin antagonist, blocks the phase advancing effects of melatonin in C3H mice
Authors: Weibel, L Rettori, MC Lesieur, D Delagrange, P Renard, P Van Reeth, O
Citation: L. Weibel et al., A single oral dose of S 22153, a melatonin antagonist, blocks the phase advancing effects of melatonin in C3H mice, BRAIN RES, 829(1-2), 1999, pp. 160-166
6-aminoalkyloxazolo[4,5-b]pyridin-2(3H)-ones: Synthesis and evaluation of antinoceptive activity
Authors: Savelon, L Bizot-Espiard, JG Caignard, DH Pfeiffer, B Renard, P Viaud, MC Guillaumet, G
Citation: L. Savelon et al., 6-aminoalkyloxazolo[4,5-b]pyridin-2(3H)-ones: Synthesis and evaluation of antinoceptive activity, BIO MED CH, 6(11), 1998, pp. 1963-1973
Pyridothiadiazinedioxides structurally related to quinazolinones cholecystokinin gastrin receptor ligands: synthesis and biological evaluation
Authors: Pirotte, B de Tullio, P Podona, T Diouf, O Dewalque, D Neven, P Masereel, B Caignard, DH Renard, P Delarge, J
Citation: B. Pirotte et al., Pyridothiadiazinedioxides structurally related to quinazolinones cholecystokinin gastrin receptor ligands: synthesis and biological evaluation, EUR J PH SC, 7(1), 1998, pp. 29-40
Melatonin, a suitable lead compound for rational drug design
Authors: Lesieur, D Leclerc, V Chavatte, P Marot, C Renard, P Guardiola-Lemaitre, B
Citation: D. Lesieur et al., Melatonin, a suitable lead compound for rational drug design, THERAPIE, 53(5), 1998, pp. 429-437
Design of new anticancer drugs. II. Easy arynic access to benzocyclobutacarbazoles, a new family of antitumor agents
Authors: Christophe, S Kuehm-Caubere, C Renard, P Pfeiffer, B Caubere, P
Citation: S. Christophe et al., Design of new anticancer drugs. II. Easy arynic access to benzocyclobutacarbazoles, a new family of antitumor agents, TETRAHEDR L, 39(51), 1998, pp. 9431-9434
Risultati: 1-25 | 26-50 | 51-65 |