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Results: 1-8 |
Results: 8
PHOSPHODIESTERASE INHIBITORY PROPERTIES OF LOSARTAN - DESIGN AND SYNTHESIS OF NEW LEAD COMPOUNDS
Authors: SEGARRA V CRESPO MI PUJOL F BELETA J DOMENECH T MIRALPEIX M PALACIOS JM CASTRO A MARTINEZ A
Citation: V. Segarra et al., PHOSPHODIESTERASE INHIBITORY PROPERTIES OF LOSARTAN - DESIGN AND SYNTHESIS OF NEW LEAD COMPOUNDS, Bioorganic & medicinal chemistry letters, 8(5), 1998, pp. 505-510
HETEROCYCLIC-FUSED 3(2H)-PYRIDAZINONES AS POTENT AND SELECTIVE PDE-IVINHIBITORS - FURTHER STRUCTURE-ACTIVITY-RELATIONSHIPS AND MOLECULAR MODELING STUDIES
Authors: DALPIAZ V GIOVANNONI MP CASTELLANA C PALACIOS JM BELETA J DOMENECH T SEGARRA V
Citation: V. Dalpiaz et al., HETEROCYCLIC-FUSED 3(2H)-PYRIDAZINONES AS POTENT AND SELECTIVE PDE-IVINHIBITORS - FURTHER STRUCTURE-ACTIVITY-RELATIONSHIPS AND MOLECULAR MODELING STUDIES, European journal of medicinal chemistry, 33(10), 1998, pp. 789-797
SURGICAL-TREATMENT FOR NEUROBLASTOMA - COMPLICATIONS DURING 15 YEARS EXPERIENCE
Authors: CANETE A JOVANI C LOPEZ A COSTA E SEGARRA V FERNANDEZ JM VERDEGUER A VELAZQUEZ J CASTEL V
Citation: A. Canete et al., SURGICAL-TREATMENT FOR NEUROBLASTOMA - COMPLICATIONS DURING 15 YEARS EXPERIENCE, Journal of pediatric surgery, 33(10), 1998, pp. 1526-1530
DESIGN, SYNTHESIS, AND BIOLOGICAL-ACTIVITIES OF NEW THIENO[3,2-D]PYRIMIDINES AS SELECTIVE TYPE-4 PHOSPHODIESTERASE INHIBITORS
Authors: CRESPO MI PAGES L VEGA A SEGARRA V LOPEZ M DOMENECH T MIRALPEIX M BELETA J RYDER H PALACIOS JM
Citation: Mi. Crespo et al., DESIGN, SYNTHESIS, AND BIOLOGICAL-ACTIVITIES OF NEW THIENO[3,2-D]PYRIMIDINES AS SELECTIVE TYPE-4 PHOSPHODIESTERASE INHIBITORS, Journal of medicinal chemistry, 41(21), 1998, pp. 4021-4035
NOVEL HETEROCYCLIC-FUSED PYRIDAZINONES AS POTENT AND SELECTIVE PHOSPHODIESTERASE-IV INHIBITORS
Authors: DALPIAZ V GIOVANNONI MP CASTELLANA C PALACIOS JM BELETA J DOMENECH T SEGARRA V
Citation: V. Dalpiaz et al., NOVEL HETEROCYCLIC-FUSED PYRIDAZINONES AS POTENT AND SELECTIVE PHOSPHODIESTERASE-IV INHIBITORS, Journal of medicinal chemistry, 40(10), 1997, pp. 1417-1421
DEGRADATION PROFILE AND IDENTIFICATION OF THE MAJOR DEGRADATION PRODUCTS OF DOBUPRIDE UNDER SEVERAL CONDITIONS BY GC MS AND HPLC-PARTICLE BEAM MS/
Authors: SEGARRA V CARRERA F FABREGAS JL CLARAMUNT J
Citation: V. Segarra et al., DEGRADATION PROFILE AND IDENTIFICATION OF THE MAJOR DEGRADATION PRODUCTS OF DOBUPRIDE UNDER SEVERAL CONDITIONS BY GC MS AND HPLC-PARTICLE BEAM MS/, Journal of pharmaceutical and biomedical analysis, 13(8), 1995, pp. 987-993
SYNTHETIC APPLICATIONS OF 2-ARYL-4-PIPERIDONES .10. SYNTHESIS OF 3-AMINOPIPENDINES, POTENTIAL SUBSTANCE-P ANTAGONISTS
Authors: DIEZ A VOLDOIRE A LOPEZ I RUBIRALTA M SEGARRA V PAGES L PALACIOS JM
Citation: A. Diez et al., SYNTHETIC APPLICATIONS OF 2-ARYL-4-PIPERIDONES .10. SYNTHESIS OF 3-AMINOPIPENDINES, POTENTIAL SUBSTANCE-P ANTAGONISTS, Tetrahedron, 51(17), 1995, pp. 5143-5156
2ND MESSENGER SYSTEMS AS TARGETS FOR NEW THERAPEUTIC AGENTS - FOCUS ON SELECTIVE PHOSPHODIESTERASE INHIBITORS
Authors: PALACIOS JM BELETA J SEGARRA V
Citation: Jm. Palacios et al., 2ND MESSENGER SYSTEMS AS TARGETS FOR NEW THERAPEUTIC AGENTS - FOCUS ON SELECTIVE PHOSPHODIESTERASE INHIBITORS, Il Farmaco, 50(12), 1995, pp. 819-827
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