M J Morcillo

Synthesis and structure-activity relationships of a new model of arylpiperazines. 5. Study of the physicochemical influence of the pharmacophore on 5-HT(1a)/alpha(1)-adrenergic receptor affinity: synthesis of a new derivative with mixed 5-HT(1a)/d(2) antagonist properties.

M L López-Rodríguez, M J Morcillo, E Fernández, 2001, Journal of medicinal chemistry.

Synthesis and structure-activity relationships of a new model of arylpiperazines. 3.1 2-[omega-(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. López-Rodríguez, M. Murcia, A. Sanz, 1997, Journal of medicinal chemistry.

Synthesis and structure-activity relationships of a new model of arylpiperazines. Study of the 5-HT(1a)/alpha(1)-adrenergic receptor affinity by classical hansch analysis, artificial neural networks, and computational simulation of ligand recognition.

L. Pardo, M. López-Rodríguez, K. Schaper, 2001, Journal of medicinal chemistry.

First pharmacophoric hypothesis for 5-HT7 antagonism.

J. Lavandera, J. Ramos, M. López-Rodríguez, 2000, Bioorganic & medicinal chemistry letters.