PUBLICATIONS
1999-1995
Benzimidazole derivatives. 1. Synthesis and structure-activity relationships of new benzimidazole-4-carboxamides and carboxylates as potent and selective 5-HT4 receptor antagonists
M.L. López Rodríguez, B. Benhamú, A. Viso, M.J. Morcillo, M. Murcia, L. Orensanz, M.J. Alfaro, M.I. Martín
Design and synthesis of 2-[4-[4-(m-(ethylsulfonamido)phenyl) piperazin-1-yl]butyl]-1,3-dioxoperhydropyrrolo[1,2-c]imidazole (EF-7412) using neural networks. A selective derivative with mixed 5-HT1A/D2 antagonist properties
M.L. López Rodríguez, M.J. Morcillo, E. Fernández, M.L. Rosado, L. Orensanz, M.E. Beneytez, J. Manzanares, J.A. Fuentes, K.J. Schaper
Benzimidazole derivatives. 2. Synthesis and structure-activity relationships of new azabicyclic benzimidazole-4-carboxylic acid derivatives with affinity for serotoninergic 5-HT3 receptors
M.L. López Rodríguez, B. Benhamú, M.J. Morcillo, I.D. Tejada, L. Orensanz, M.J. Alfaro, M.I. Martín
Benzimidazole derivatives. 1. Synthesis and structure-activity relationships of new benzimidazole-4-carboxamides and carboxylates as potent and selective 5-HT4 receptor antagonists
M.L. López Rodríguez, A. Viso, B. Benhamú, J.L. Rominguera, M. Murcia
Design and synthesis of 2-[4-[4-(m-(ethylsulfonamido)phenyl) piperazin-1-yl]butyl]-1,3-dioxoperhydropyrrolo[1,2-c]imidazole (EF-7412) using neural networks. A selective derivative with mixed 5-HT1A/D2 antagonist properties
M.L. López Rodríguez, M.J. Morcillo, T.K. Rovat, E. Fernández, B. Vicente, A.M. Sanz, M. Hernández, L. Orensanz
Benzimidazole derivatives. 2. Synthesis and structure-activity relationships of new azabicyclic benzimidazole-4-carboxylic acid derivatives with affinity for serotoninergic 5-HT3 receptors
M.L. López Rodríguez, M.J. Morcillo, T.K. Rovat, E. Fernández, A.M. Sanz, L. Orensanz
Preclinical pharmacology of B-20991, a 5-HT1A receptor agonist with anxiolytic activity
M.E. Beneytez, M.L. López Rodríguez, M.L. Rosado, M.J. Morcillo, L. Orensanz, J.A. Fuentes, J. Manzanares
Comparative receptor mapping of serotoninergic 5-HT3 and 5-HT4 binding sites
M.L. López Rodríguez, M.J. Morcillo, B. Benhamú, M.L. Rosado
Synthesis and structure-activity relationships of a new model of arylpiperazines. 2. Three-dimensional quantitative structure-activity relationships of hydantoin-phenylpiperazine derivatives with affnity for 5-HT1A and 1 receptors. A comparison of CoMFA models
M.L. López Rodríguez, M.L. Rosado, B. Benhamú, M.J. Morcillo, E. Fernández, K.J. Schaper
Synthesis and structure-activity relationships of a new model of arylpiperazines. 3. 2-['-(4-Arylpiperazin-1-yl) alkyl]perhydropyrrolo[1,2-c]imidazoles and -perhydroimidazo[1,5-a]pyridines: Study of the influence of the terminal amide fragment on 5-HT1A affinity/selectivity
M.L. López Rodríguez, M.J. Morcillo, E. Fernández, E. Porras, M. Murcia, A.M. Sanz, L. Orensanz
Synthesis and structure-activity relationships of a new model of arylpiperazines. 1. 2-[[4-(o-methoxyphenyl)piperazin-1-yl]methyl]-1,3-dioxoperhydroimidazo[1,5-alpha]pyridine: a selective 5-HT1A receptor agonist
M.L. López-Rodríguez, M.L. Rosado, B. Benhamú, M.J. Morcill, A.M. Sanz, L. Orensanz, M.E. Beneitez, J.A. Fuentes, J. Manzanares
Alpha1-adrenoceptor reagents.Synthesis of some 5,6,11,11a-tetrahydro-1H-imidazo[1',5':1,6]pyrido and 5,6,11,11b-tetrahydro-1H-imidazo[1',5':1,2]pyrido[3,4-b]indole-1,3(2H)-diones
M.L. Lopez-Rodriguez, M.J. Morcillo, B. Benhamu, E. Fernandez, J. Serrano, L. Orensanz.