Authors:
FINIZIA G
DONATI D
PENTASSUGLIA G
POLINELLI S
TARZIA G
TRANQUILLINI ME
URSINI A
Citation: G. Finizia et al., SYNTHESIS AND EVALUATION OF 1,5-BENZODIAZEPINES WITH BRIDGED CYCLOALKYL SUBSTITUENTS AT THE N-1 POSITION AS POTENT AND SELECTIVE CCK-B LIGANDS, Archiv der pharmazie, 331(1), 1998, pp. 41-44
Authors:
ARALDI GL
DONATI D
TRANQUILLINI ME
URSINI A
Citation: Gl. Araldi et al., DIASTEREOMERIC SEPARATION OF 1,5-BENZODIAZEPINES DUE TO THE PRESENCE OF A CHIRAL CENTER ON THE N-5 ALKYLIC CHAIN, Il Farmaco, 53(1), 1998, pp. 49-54
Authors:
CORSI M
OLIOSI B
VANAMSTERDAM FTM
ANTOLINI M
MELOTTO S
GERRARD P
MARAIA G
REGGIANI A
URSINI A
DONATI D
GAVIRAGHI G
RATTI E
TRIST DG
Citation: M. Corsi et al., PHARMACOLOGICAL CHARACTERIZATION OF GV191869X - A NOVEL, POTENT AND SELECTIVE CCK-B RECEPTOR ANTAGONIST, British Journal of Pharmacology, 123, 1998, pp. 249-249
Authors:
TRANQUILLINI ME
CASSARA PG
CORSI M
CUROTTO C
DONATI D
FINIZIA G
PENTASSUGLIA G
POLINELLI S
TARZIA G
URSINI A
VANAMSTERDAM FTM
Citation: Me. Tranquillini et al., NOVEL 1,5-BENZODIAZEPINES AS CCK-B LIGANDS - EFFECT OF ARYL-CARBAMIC SUBSTITUENTS AT THE C-3 POSITION TOGETHER WITH HALOGEN SUBSTITUTION ONTHE BENZO-FUSED RING, Archiv der pharmazie, 330(11), 1997, pp. 353-357
Citation: G. Curotto et al., A CHEMICAL METHOD FOR THE PREPARATION OF NOVEL 1,5-BENZODIAZEPINES ACTING AS CCK-B ANTAGONISTS IN HIGH ENANTIOMERIC PURITY, Tetrahedron, 53(21), 1997, pp. 7347-7364
Authors:
PENTASSUGLIA G
ARALDI GL
DONATI D
FERIANI A
OLIOSI B
PASQUARELLO A
URSINI A
Citation: G. Pentassuglia et al., SYNTHESIS OF 5-MEMBERED RING-TYPE COMPOUNDS AS POTENTIAL CHOLECYSTOKININ RECEPTOR LIGANDS, Il Farmaco, 52(10), 1997, pp. 573-581
Authors:
FINIZIA G
DONATI D
OLIOSI B
TRANQUILLINI ME
URSINI A
Citation: G. Finizia et al., SYNTHESIS AND EVALUATION OF NOVEL 1,5-BENZODIAZEPINES AS POTENT AND SELECTIVE CCK-B LIGANDS - EFFECT OF THE SUBSTITUTION OF THE N-5 PHENYL WITH ALKYL-GROUPS, Bioorganic & medicinal chemistry letters, 6(24), 1996, pp. 2957-2962
Authors:
ARALDI G
DONATI D
OLIOSI B
PASQUARELLO A
POLINELLI S
TARZIA G
URSINI A
VANAMSTERDAM FTM
Citation: G. Araldi et al., SYNTHESIS AND RECEPTOR-BINDING AFFINITY OF DIPEPTOID CHOLECYSTOKININ LIGANDS, European journal of medicinal chemistry, 31(3), 1996, pp. 215-220
Authors:
PENTASSUGLIA G
BERTANI B
DONATI D
URSINI A
Citation: G. Pentassuglia et al., L-PHENYL-4(1H)-QUINAZOLINONES AND 2,3-DIHYDRO-1-PHENYL-4(1H)-QUINAZOLINONES AS POTENTIAL CHOLECYSTOKININ RECEPTOR LIGANDS, Journal of heterocyclic chemistry, 33(4), 1996, pp. 1163-1170
Authors:
ARALDI G
DONATI D
OLIOSI B
URSINI A
VANAMSTERDAM F
NATALINI B
PELLICCIARI R
TARZIA G
Citation: G. Araldi et al., SYNTHESIS AND RECEPTOR-BINDING AFFINITY OF CHOLECYSTOKININ RECEPTOR LIGANDS - 2-INDOLYL AND 1-INDOLYL DERIVATIVES OF PD134308, Il Farmaco, 51(7), 1996, pp. 471-476
Authors:
CUROTTO G
DONATI D
PENTASSUGLIA G
URSINI A
Citation: G. Curotto et al., 1,5-BENZODIAZEPINES AS CCK-B ANTAGONISTS - EFFECT OF HALOGEN SUBSTITUTION AT THE BENZO-FUSED RING ON POTENCY AND SELECTIVITY, Bioorganic & medicinal chemistry letters, 5(24), 1995, pp. 3011-3016
Citation: G. Curotto et al., A NEW METHOD FOR THE RESOLUTION OF AMINES AND ITS APPLICATION TO 3-AMINO-1,5-BENZODIAZEPINES, Tetrahedron : asymmetry, 6(4), 1995, pp. 849-852
Authors:
PENTASSUGLIA G
TARZIA G
ANDREOTTI D
BISMARA C
CARLESSO R
DONATI D
GAVIRAGHI G
PERBONI A
PEZZOLI A
ROSSI T
TAMBURINI B
URSINI A
Citation: G. Pentassuglia et al., SYNTHESIS OF NOVEL 6-ALPHA AND 6-BETA-ALKYLCARBONYLMETHYL SUBSTITUTEDPENEMS, Journal of antibiotics, 48(5), 1995, pp. 399-407
Authors:
CORSI M
DALFORNO G
VANAMSTERDAM FTM
FERIANI A
URSINI A
RATTI E
GAVIRAGHI G
TRIST DG
Citation: M. Corsi et al., THE CHARACTERIZATION IN FUNCTIONAL ASSAYS OF GV-150013 - A NOVEL CCK-B RECEPTOR ANTAGONIST, British Journal of Pharmacology, 114, 1995, pp. 91-91
Authors:
PELLICCIARI R
NATALINI B
SADEGHPOUR BM
ROSATO GC
URSINI A
Citation: R. Pellicciari et al., THE REACTION OF ALPHA-DIAZO-BETA-HYDROXY ESTERS WITH BORON-TRIFLUORIDE, Journal of the Chemical Society, Chemical Communications, (24), 1993, pp. 1798-1800