Authors:
Schenone, S
Bruno, O
Ranise, A
Bondavalli, F
Filippelli, W
Falcone, G
Giordano, L
Vitelli, MR
Citation: S. Schenone et al., 3-arylsulphonyl-5-arylamino-1,3,4-thiadiazol-2(3H)ones as anti-inflammatory and analgesic agents, BIO MED CH, 9(8), 2001, pp. 2149-2153
Authors:
Bruno, O
Schenone, S
Ranise, A
Bondavalli, F
Barocelli, E
Ballabeni, V
Chiavarini, M
Bertoni, S
Tognolini, M
Impicciatore, M
Citation: O. Bruno et al., New polycyclic pyrimidine derivatives with antiplatelet in vitro activity:Synthesis and pharmacological screening, BIO MED CH, 9(3), 2001, pp. 629-636
Authors:
Schenone, S
Bruno, O
Fossa, P
Ranise, A
Menozzi, G
Mosti, L
Bondavalli, F
Martini, C
Trincavelli, L
Citation: S. Schenone et al., Synthesis and biological data of 4-amino-1-(2-chloro-2-phenylethyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl esters, a new series of A(1)-adenosine receptor (A(1)AR) ligands, BIOORG MED, 11(18), 2001, pp. 2529-2531
Authors:
Bruno, O
Brullo, C
Ranise, A
Schenone, S
Bondavalli, F
Barocelli, E
Ballabeni, V
Chiavarini, M
Tognolini, V
Impicciatore, M
Citation: O. Bruno et al., Synthesis and pharmacological evaluation of 2,5-cycloamino-5H[1]benzopyrano[4,3-d]pyrimidines endowed with in vitro antiplatelet activity, BIOORG MED, 11(11), 2001, pp. 1397-1400
Authors:
Schenone, S
Bruno, O
Ranise, A
Bondavalli, F
Filippelli, W
Falcone, G
Rinaldi, B
Citation: S. Schenone et al., O-[2-Hydroxy-3-(dialkylamino)propyl]ethers of (+)-1,7,7-trimethyl bicyclo[2.2.1]heptan-2-one oxime (camphor oxime) with analgesic and antiarrhythmic activities, FARMACO, 55(6-7), 2000, pp. 495-498
Authors:
Schenone, S
Bruno, O
Ranise, A
Bondavalli, F
Falcone, G
Filippelli, W
Rivaldi, B
Citation: S. Schenone et al., N-Substituted 3-(arylamino)-4,5-dihydro-2H-benz[g]indazol-2-yl acetamides with anti-inflammatory and analgesic activities, FARMACO, 55(5), 2000, pp. 383-388
Authors:
Bondavalli, F
Bruno, O
Lo Presti, E
Menozzi, G
Mosti, L
Citation: F. Bondavalli et al., An efficient synthesis of functionalized 2-pyridones by direct route or via amide/enolate ammonium salt intermediates, SYNTHESIS-S, (7), 1999, pp. 1169-1174
Authors:
Bruno, O
Schenone, S
Ranise, A
Bondavalli, F
Filippelli, W
Falcone, G
Motola, G
Mazzeo, F
Citation: O. Bruno et al., Antiinflammatory agents: new series of N-substituted amino acids with complex pyrimidine structures endowed with antiphlogistic activity, FARMACO, 54(1-2), 1999, pp. 95-100
Authors:
Schenone, S
Bruno, O
Ranise, A
Bondavalli, F
Filippelli, W
Falcone, G
Piucci, B
Sorrentino, S
Citation: S. Schenone et al., Preparation of new 5-aroylamino substituted 3-nicotinoyl/isonicotinoyl-1,3,4-thiadiazol-2(3H)-ones with anti-inflammatory activity, FARMACO, 53(8-9), 1998, pp. 586-589
Authors:
Schenone, S
Bruno, O
Ranise, A
Bondavalli, F
Filippelli, W
Rossi, F
Falcone, G
Citation: S. Schenone et al., Synthesis and anti-inflammatory activity of esters derived from 5-aryl-1,2-dihydro-2-(2-hydroxyethyl)-3H-1,2,4-triazole-3-thiones, FARMACO, 53(8-9), 1998, pp. 590-593