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Authors: MINARINI A BUDRIESI R CHIARINI A LEONARDI A MELCHIORRE C
Citation: A. Minarini et al., SEARCH FOR ALPHA(1)-ADRENOCEPTOR SUBTYPES SELECTIVE ANTAGONISTS - DESIGN, SYNTHESIS AND BIOLOGICAL-ACTIVITY OF CYSTAZOSIN, AN ALPHA(1D)-ADRENOCEPTOR ANTAGONIST, Bioorganic & medicinal chemistry letters, 8(11), 1998, pp. 1353-1358

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: QUAGLIA W GIANNELLA M PIERGENTILI A PIGINI M BRASILI L DITORO R ROSSETTI L SPAMPINATO S MELCHIORRE C
Citation: W. Quaglia et al., -DIHYDROSPIRO[2H-1-BENZOTHIOPYRAN-2,4'-PIPERIDINE] (SPIPETHIANE), A POTENT AND HIGHLY SELECTIVE SIGMA(1) LIGAND, Journal of medicinal chemistry, 41(10), 1998, pp. 1557-1560

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: GIARDINA D CRUCIANELLI M MARUCCI G ANGELI P MELCHIORRE C ANTOLINI L
Citation: D. Giardina et al., SYNTHESIS AND ALPHA-ADRENOCEPTOR BLOCKING ACTIVITY OF THE ENANTIOMERSOF ROETHYL)-[2-(2-METHOXYPHENOXY)-1-METHYLETHYL]AMINE HYDROCHLORIDE, Bioorganic & medicinal chemistry, 5(9), 1997, pp. 1775-1782

Authors: GIARDINA D CRUCIANELLI M GULINI U MARUCCI G MELCHIORRE C SPAMPINATO S
Citation: D. Giardina et al., SYNTHESIS AND ALPHA(1)-ANTAGONIST ACTIVITY OF NEW PRAZOSIN-RELATED AND BENEXTRAMINE-RELATED TETRAAMINE DISULFIDES, European journal of medicinal chemistry, 32(1), 1997, pp. 9-20

Authors: GIARDINA D CRUCIANELLI M ROMANELLI R LEONARDI A POGGESI E MELCHIORRE C
Citation: D. Giardina et al., SYNTHESIS AND BIOLOGICAL PROFILE OF THE ENANTIOMERS OF HOXYQUINAZOLIN-2-YL)-CIS-OCTAHYDROQUINOXALIN-1-YL] FURAN-2-YLMETHANONE (CYCLAZOSIN),A POTENT COMPETITIVE ALPHA(1B)-ADRENOCEPTOR ANTAGONIST, Journal of medicinal chemistry, 39(23), 1996, pp. 4602-4607

Authors: QUAGLIA W PIGINI M TAYEBATI SK PIERGENTILI A GIANNELLA M LEONARDI A TADDEI C MELCHIORRE C
Citation: W. Quaglia et al., SYNTHESIS, ABSOLUTE-CONFIGURATION, AND BIOLOGICAL PROFILE OF THE ENANTIOMERS OF OLYL-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL)METHYL]AMINE (MEPHENDIOXAN), A POTENT COMPETITIVE ALPHA(1A)-ADRENOCEPTOR ANTAGONIST, Journal of medicinal chemistry, 39(11), 1996, pp. 2253-2258

Authors: QUAGLIA W GIANNELLA M MARUCCI G PIERGENTILI A PIGINI M TAYEBATI SK MELCHIORRE C
Citation: W. Quaglia et al., STRUCTURE-ACTIVITY-RELATIONSHIPS IN 1,4-BENZODIOXAN-RELATED COMPOUNDS.5. EFFECTS OF MODIFICATION OF THE SIDE-CHAIN ON ALPHA-ADRENOCEPTOR BLOCKING ACTIVITY, Il Farmaco, 51(1), 1996, pp. 27-32

Authors: GIARDINA D CRUCIANELLI M MARUCCI G MELCHIORRE C POLIDORI C POMPEI P MASSI M
Citation: D. Giardina et al., PHARMACOLOGICAL EVALUATION OF PRAZOSIN-RELATED AND DOXAZOSIN-RELATED COMPOUNDS WITH MODIFIED PIPERAZINE RING, Arzneimittel-Forschung, 46(11), 1996, pp. 1054-1059

Authors: MELCHIORRE C MINARINI A SPAMPINATO S TUMIATTI V
Citation: C. Melchiorre et al., DESIGN, SYNTHESIS AND BIOLOGICAL-ACTIVITY OF SOME TETRAAMINES RELATEDTO METHOCTRAMINE AND 4-DAMP, Bioorganic & medicinal chemistry letters, 5(8), 1995, pp. 785-790

Authors: TUMIATTI V SPAMPINATO S RECANATINI M MINARINI A MELCHIORRE C CHIARINI A BUDRIESI R
Citation: V. Tumiatti et al., DESIGN, SYNTHESIS AND BIOLOGICAL-ACTIVITY OF SOME 4-DAMP-RELATED COMPOUNDS, Bioorganic & medicinal chemistry letters, 5(20), 1995, pp. 2325-2330

Authors: ANGELI P CANTALAMESSA F GULINI U MELCHIORRE C
Citation: P. Angeli et al., SELECTIVE BLOCKADE OF MUSCARINIC M(2) RECEPTORS IN-VIVO BY THE NEW ANTAGONIST TRIPITRAMINE, Naunyn-Schmiedeberg's archives of pharmacology, 352(3), 1995, pp. 304-307

Authors: MELCHIORRE C MINARINI A BUDRIESI R CHIARINI A SPAMPINATO S TUMIATTI V
Citation: C. Melchiorre et al., THE DESIGN OF NOVEL METHOCTRAMINE-RELATED TETRAAMINES AS MUSCARINIC RECEPTOR SUBTYPE-SELECTIVE ANTAGONISTS, Life sciences, 56(11-12), 1995, pp. 837-844

Authors: CANTALAMESSA F ANGELI P MELCHIORRE C
Citation: F. Cantalamessa et al., TRIPITRAMINE - FURTHER PHARMACOLOGICAL EVALUATION IN PITHED RAT, Life sciences, 56(11-12), 1995, pp. 1012-1012

Authors: GIARDINA D CRUCIANELLI M MELCHIORRE C TADDEI C TESTA R
Citation: D. Giardina et al., RECEPTOR-BINDING PROFILE OF CYCLAZOSIN, A NEW ALPHA(1B)-ADRENOCEPTOR ANTAGONIST, European journal of pharmacology, 287(1), 1995, pp. 13-16

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: SABATINO P RECANATINI M TUMIATTI V MELCHIORRE C
Citation: P. Sabatino et al., STRUCTURAL STUDIES ON THE ANTIMUSCARINIC AGENTS SPIRO-DAMP AND HYDROXY-DAMP, AND COMPARISON WITH RELATED-COMPOUNDS, Acta crystallographica. Section C, Crystal structure communications, 50, 1994, pp. 640-645

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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