Authors: Pinna, GA Curzu, MM Murineddu, G Chelucci, G Cignarella, G Menta, E Krell, HW Rastelli, G Ferrari, AM

Citation: Ga. Pinna et al., Preparation of thieno[3,2-h]cinnolinones as matrix metalloproteinase inhibitors, ARCH PHARM, 333(2-3), 2000, pp. 37-47

Authors: Pinna, GA Murineddu, G Curzu, MM Villa, S Vianello, P Borea, PA Gessi, S Toma, L Colombo, D Cignarella, G

Citation: Ga. Pinna et al., Synthesis, modelling, and mu-opioid receptor affinity of N-3(9)-arylpropenyl-N-9(3)-propionyl-3,9-diazabicyclo[3.3.1]nonanes, FARMACO, 55(8), 2000, pp. 553-562

Authors: Villa, S Cignarella, G Curzu, MM Pinna, GA Pini, E Toma, L

Citation: S. Villa et al., Behaviour of 5,6-dihydrothieno[2,3-h]cinnolin-3(2H)-one and 5,6-dihydrothieno[3,2-h]cinnolin-3(2H)-one towards hydrazine. Synthesis of thienocinnolinones and of 4-aminothienocinnolinones, J HETERO CH, 36(5), 1999, pp. 1253-1257

Authors: Villa, S Evoli, GL Cignarella, G Curzu, MM Pinna, GA

Citation: S. Villa et al., Behavior of 5,6-dihydrobenzo[h]cinnolinones towards hydrazine. Synthesis of benzo[h]cinnolinones and of 4-aminobenzo[h]cinnolinones, J HETERO CH, 36(2), 1999, pp. 485-492

Authors: Pinna, GRA Curzu, MM Sechi, M Chelucci, G Maciocco, E

Citation: Gra. Pinna et al., Synthesis and dopamine D-2-Iike receptor binding affinity of substituted 5-phenyl-pyrrole-3-carboxamides, FARMACO, 54(8), 1999, pp. 542-550

Authors: Pinna, GA Curzu, MM Sechi, M Chelucci, G Vianello, P Maciocco, E

Citation: Ga. Pinna et al., Synthesis and D-2-like binding affinity of 4,5-dihydro-1H-benzo[g]indole-3-carboxamide derivatives as conformationally restricted 5-phenyl-pyrrole-3-carboxamide analogs, FARMACO, 53(10-11), 1998, pp. 684-689