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Results: 1-7 |
Results: 7
1,5-benzodiazepine tricyclic derivatives exerting anti-inflammatory effects in mice by inhibiting interleukin-6 and prostaglandin E-2 production
Authors: Fruscella, P Sottocorno, M Di Braccio, M Diomede, L Piccardi, N Cagnotto, A Grossi, G Romano, M Mennini, T Roma, G
Citation: P. Fruscella et al., 1,5-benzodiazepine tricyclic derivatives exerting anti-inflammatory effects in mice by inhibiting interleukin-6 and prostaglandin E-2 production, PHARMAC RES, 43(5), 2001, pp. 445-451
Synthesis, antiplatelet activity and comparative molecular field analysis of substituted 2-amino-4H-pyrido[1,2-a]pyrimidin-ones, their congeners and isosteric analogues (vol 8, pg 751, 2000)
Authors: Roma, G Cinone, N Di Braccio, M Grossi, G Leoncini, G Signorello, MG Carotti, A
Citation: G. Roma et al., Synthesis, antiplatelet activity and comparative molecular field analysis of substituted 2-amino-4H-pyrido[1,2-a]pyrimidin-ones, their congeners and isosteric analogues (vol 8, pg 751, 2000), BIO MED CH, 9(2), 2001, pp. 555-555
Oxygen self-diffusion in alpha-quartz
Authors: Roma, G Limoge, Y Baroni, S
Citation: G. Roma et al., Oxygen self-diffusion in alpha-quartz, PHYS REV L, 86(20), 2001, pp. 4564-4567
Synthesis, antiplatelet activity and comparative molecular field analysis of substituted 2-amino4H-pyrido[1,2-a]pyrimidin-4-ones, their congeners andisosteric analogues
Authors: Roma, G Cinone, N Di Braccio, M Grossi, G Leoncini, G Signorello, MG Carott, A
Citation: G. Roma et al., Synthesis, antiplatelet activity and comparative molecular field analysis of substituted 2-amino4H-pyrido[1,2-a]pyrimidin-4-ones, their congeners andisosteric analogues, BIO MED CH, 8(4), 2000, pp. 751-768
1,8-naphthyridines IV. 9-substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities
Authors: Roma, G Di Braccio, M Grossi, G Mattioli, F Ghia, M
Citation: G. Roma et al., 1,8-naphthyridines IV. 9-substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities, EUR J MED C, 35(11), 2000, pp. 1021-1035
8-chloro-6-phenyl-4H-[1,2,4]-triazolo[4,3-a][1,5]benzodiazepin-5(6H)-one
Authors: Borassi, A Carnasciali, MM Mugnoli, A Roma, G
Citation: A. Borassi et al., 8-chloro-6-phenyl-4H-[1,2,4]-triazolo[4,3-a][1,5]benzodiazepin-5(6H)-one, ACT CRYST C, 56, 2000, pp. 258-259
Acid-catalysed hydrolysis and benzodiazepine-like properties of 5-(dialkylamino)- and 5-(alkylthio)-substituted 8-chloro-6-phenyl-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepines in mice
Authors: Caccia, S Grossi, G Fracasso, C Nacca, A Cagnotto, A Mennini, T Ghia, M Roma, G
Citation: S. Caccia et al., Acid-catalysed hydrolysis and benzodiazepine-like properties of 5-(dialkylamino)- and 5-(alkylthio)-substituted 8-chloro-6-phenyl-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepines in mice, J PHARM PHA, 50(7), 1998, pp. 723-728
Risultati: 1-7 |