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Results: 10

Authors: BOLOGNESI ML BUDRIESI R CHIARINI A POGGESI E LEONARDI A MELCHIORRE C
Citation: Ml. Bolognesi et al., DESIGN, SYNTHESIS, AND BIOLOGICAL-ACTIVITY OF PRAZOSIN-RELATED ANTAGONISTS - ROLE OF THE PIPERAZINE AND FURAN UNITS OF PRAZOSIN ON THE SELECTIVITY FOR ALPHA(1)-ADRENORECEPTOR SUBTYPES, Journal of medicinal chemistry, 41(24), 1998, pp. 4844-4853

Authors: MELCHIORRE C ANDRISANO V BOLOGNESI ML BUDRIESI R CAVALLI A CAVRINI V ROSINI M TUMIATTI V RECANATINI M
Citation: C. Melchiorre et al., ACETYLCHOLINESTERASE NONCOVALENT INHIBITORS BASED ON A POLYAMINE BACKBONE FOR POTENTIAL USE AGAINST ALZHEIMERS-DISEASE, Journal of medicinal chemistry, 41(22), 1998, pp. 4186-4189

Authors: BOLOGNESI ML MINARINI A BUDRIESI R CACCIAGUERRA S CHIARINI A SPAMPINATO S TUMIATTI V MELCHIORRE C
Citation: Ml. Bolognesi et al., UNIVERSAL TEMPLATE APPROACH TO DRUG DESIGN - POLYAMINES AS SELECTIVE MUSCARINIC RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 41(21), 1998, pp. 4150-4160

Authors: MELCHIORRE C BOLOGNESI ML BUDRIESI R CHIARINI A GIARDINA D MINARINI A QUAGLIA W LEONARDI A
Citation: C. Melchiorre et al., SEARCH FOR SELECTIVE ANTAGONISTS AT ALPHA(1)-ADRENORECEPTORS - NEUTRAL OR NEGATIVE ANTAGONISM, Il Farmaco, 53(4), 1998, pp. 278-286

Authors: BARBIER P COLELLI A BOLOGNESI ML MINARINI A TUMIATTI V CORSINI GU MELCHIORRE C MAGGIO R
Citation: P. Barbier et al., ANTAGONIST BINDING PROFILE OF THE SPLIT CHIMERIC MUSCARINIC M2-TRUNC M3-TAIL RECEPTOR/, European journal of pharmacology, 355(2-3), 1998, pp. 267-274

Authors: CHIARINI A BUDRIESI R BOLOGNESI ML MINARINI A MELCHIORRE C
Citation: A. Chiarini et al., IN-VITRO CHARACTERIZATION OF TRIPITRAMINE, A POLYMETHYLENE TETRAAMINEDISPLAYING HIGH SELECTIVITY AND AFFINITY FOR MUSCARINIC M(2) RECEPTORS, British Journal of Pharmacology, 114(7), 1995, pp. 1507-1517

Authors: MAGGIO R BARBIER P BOLOGNESI ML MINARINI A TEDESCHI D MELCHIORRE C
Citation: R. Maggio et al., BINDING PROFILE OF THE SELECTIVE MUSCARINIC RECEPTOR ANTAGONIST TRIPITRAMINE, European journal of pharmacology. Molecular pharmacology section, 268(3), 1994, pp. 459-462

Authors: MINARINI A BOLOGNESI ML BUDRIESI R CANOSSA M CHIARINI A SPAMPINATO S MELCHIORRE C
Citation: A. Minarini et al., DESIGN, SYNTHESIS, AND BIOLOGICAL-ACTIVITY OF METHOCTRAMINE-RELATED TETRAAMINES BEARING AN 1-DIHYDRO-6H-PYRIDO[2,3-B][1,4]BENZODIAZEPIN-6-ONE MOIETY - STRUCTURAL REQUIREMENTS FOR OPTIMUM OCCUPANCY OF MUSCARINIC RECEPTOR SUBTYPES AS REVEALED BY SYMMETRICAL AND UNSYMMETRICAL POLYAMINES, Journal of medicinal chemistry, 37(20), 1994, pp. 3363-3372

Authors: MELCHIORRE C ROMUALDI P BOLOGNESI ML DONATINI A FERRI S
Citation: C. Melchiorre et al., BINDING PROFILE OF BENEXTRAMINE AT NEUROPEPTIDE-Y RECEPTOR SUBTYPES IN RAT-BRAIN AREAS, European journal of pharmacology, 265(1-2), 1994, pp. 93-98

Authors: MELCHIORRE C BOLOGNESI ML CHIARINI A MINARINI A SPAMPINATO S
Citation: C. Melchiorre et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF SOME METHOCTRAMINE-RELATED TETRAAMINES BEARING A -DIHYDRO-6H-PYRIDO[2,3-B][1,4]-BENZODIAZEPIN-6-ONE MOIETY AS ANTIMUSCARINICS - A 2ND-GENERATION OF HIGHLY SELECTIVE M(2)-MUSCARINIC RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 36(23), 1993, pp. 3734-3737
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