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Results: 10

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
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