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Results: 1-12 |
Results: 12
Synthesis of anticonvulsive AMPA antagonists: 4-oxo-10-substituted-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives
Authors: Stutzmann, JM Bohme, GA Boireau, A Damour, D Debono, MW Genevois-Borella, A Jimonet, P Pratt, J Randle, JCR Ribeill, Y Vuilhorgne, M Mignani, S
Citation: Jm. Stutzmann et al., Synthesis of anticonvulsive AMPA antagonists: 4-oxo-10-substituted-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives, BIOORG MED, 11(9), 2001, pp. 1205-1210
Bioisosteres of 9-carboxymethyl-4-oxo-imidazo[1,2-a]indeno-[1,2-e]pyrazin-2-carboxylic acid derivatives. Progress towards selective, potent in vivo AMPA antagonists with longer durations of action
Authors: Jimonet, P Bohme, GA Bouquerel, J Boireau, A Damour, D Debono, MW Genevois-Borella, A Hardy, JC Hubert, P Manfre, F Nemecek, P Pratt, J Randle, JCR Ribeill, Y Stutzmann, JM Vuilhorgne, M Mignani, S
Citation: P. Jimonet et al., Bioisosteres of 9-carboxymethyl-4-oxo-imidazo[1,2-a]indeno-[1,2-e]pyrazin-2-carboxylic acid derivatives. Progress towards selective, potent in vivo AMPA antagonists with longer durations of action, BIOORG MED, 11(2), 2001, pp. 127-132
A convenient one-pot synthesis of phosphino-dipeptide analogs
Authors: Cristau, HJ Coulombeau, A Genevois-Borella, A Pirat, JL
Citation: Hj. Cristau et al., A convenient one-pot synthesis of phosphino-dipeptide analogs, TETRAHEDR L, 42(27), 2001, pp. 4491-4494
8-Methylureido-10-amino-10-methyl-imidazo[1,2-a]indeno[1,2-e] pyrazine-4-ones: Highly in vivo potent and selective AMPA receptor antagonists
Authors: Jimonet, P Cheve, M Bohme, GA Boireau, A Damour, D Debono, MW Genevois-Borella, A Imperato, A Pratt, J Randle, JCR Ribeill, Y Stutzmann, JM Vuilhorgne, M Mignani, S
Citation: P. Jimonet et al., 8-Methylureido-10-amino-10-methyl-imidazo[1,2-a]indeno[1,2-e] pyrazine-4-ones: Highly in vivo potent and selective AMPA receptor antagonists, BIO MED CH, 8(8), 2000, pp. 2211-2217
8-Methylureido-4,5-dihyro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazines: Highly potent in vivo AMPA antagonists
Authors: Mignani, S Bohme, GA Boireau, A Cheve, M Damour, D Debono, MW Genevois-Borella, A Imperato, A Jimonet, P Pratt, J Randle, JCR Ribeill, Y Vuilhorgne, M Stutzmann, JM
Citation: S. Mignani et al., 8-Methylureido-4,5-dihyro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazines: Highly potent in vivo AMPA antagonists, BIOORG MED, 10(6), 2000, pp. 591-596
Synthesis and potent anticonvulsant activities of 4-oxo-imidazo[1,2-a]indeno[1,2-e]pyrazin-8-and-9-carboxylic (acetic) acid AMPA antagonists
Authors: Pratt, J Jimonet, P Bohme, GA Boireau, A Damour, D Debono, MW Genevois-Borella, A Randle, JCR Ribeill, Y Stutzmann, JM Vuilhorgne, M Mignani, S
Citation: J. Pratt et al., Synthesis and potent anticonvulsant activities of 4-oxo-imidazo[1,2-a]indeno[1,2-e]pyrazin-8-and-9-carboxylic (acetic) acid AMPA antagonists, BIOORG MED, 10(24), 2000, pp. 2749-2754
4,10-dihydro-4-oxo-4H-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acidderivatives: Highly potent and selective AMPA receptors antagonists with in vivo activity
Authors: Stutzmann, JM Bohme, GA Boireau, A Damour, D Debono, MW Genevois-Borella, A Imperato, A Jimonet, P Pratt, J Randle, JCR Ribeill, Y Vuilhorgne, M Mignani, S
Citation: Jm. Stutzmann et al., 4,10-dihydro-4-oxo-4H-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acidderivatives: Highly potent and selective AMPA receptors antagonists with in vivo activity, BIOORG MED, 10(10), 2000, pp. 1133-1137
Indeno[1,2-b]pyrazin-2,3-diones: A new class of antagonists at the glycinesite of the NMDA receptor with potent in vivo activity
Authors: Jimonet, P Ribeill, Y Bohme, GA Boireau, A Cheve, M Damour, D Doble, A Genevois-Borella, A Herman, F Imperato, A Le Guern, S Manfre, F Pratt, J Randle, JCR Stutzmann, JM Mignani, S
Citation: P. Jimonet et al., Indeno[1,2-b]pyrazin-2,3-diones: A new class of antagonists at the glycinesite of the NMDA receptor with potent in vivo activity, J MED CHEM, 43(12), 2000, pp. 2371-2381
Spiro-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one derivatives are mixed AMPAand NMDA glycine-site antagonists active in vivo.
Authors: Jimonet, P Boireau, A Cheve, M Damour, D Genevois-Borella, A Imperato, A Pratt, J Randle, JCR Ribeill, Y Stutzmann, JM Mignani, S
Citation: P. Jimonet et al., Spiro-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one derivatives are mixed AMPAand NMDA glycine-site antagonists active in vivo., BIOORG MED, 9(20), 1999, pp. 2921-2926
A preparative route to fused indeno[1,2-e][1,2,4]-triazolo[4,3-a]pyrazin-4-ones
Authors: Ribeill, Y Genevois-Borella, A Vuilhorgne, M Mignani, S
Citation: Y. Ribeill et al., A preparative route to fused indeno[1,2-e][1,2,4]-triazolo[4,3-a]pyrazin-4-ones, HETEROCYCLE, 51(12), 1999, pp. 2977-2982
An efficient preparative route to fused imidazo[1,2-a]pyrazin-4-one derivatives
Authors: Damour, D Aloup, JC Barreau, M Genevois-Borella, A Jimonet, P Leconte, JP Ribeill, Y Vuilhorgne, M Mignani, S
Citation: D. Damour et al., An efficient preparative route to fused imidazo[1,2-a]pyrazin-4-one derivatives, HETEROCYCLE, 50(1), 1999, pp. 259-267
Synthesis and pharmacological properties of 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one, a new competitive AMPA/KA receptor antagonist
Authors: Mignani, S Aloup, JC Barreau, M Blanchard, JC Bohme, GA Boireau, A Damour, D Debono, MW Dubroeucq, MC Genevois-Borella, A Imperato, A Jimonet, P Pratt, J Randle, JCR Reibaud, M Ribeill, Y Stutzmann, JM
Citation: S. Mignani et al., Synthesis and pharmacological properties of 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one, a new competitive AMPA/KA receptor antagonist, DRUG DEV R, 48(3), 1999, pp. 121-129
Risultati: 1-12 |