Concepedia

Author

M. J. MORCILLO

Universidad Nacional de Educación a Distancia

Also Known As

M José Morcillo, M. J. MORCILLO, M. J. Morcillo, M. Jose MORCILLO, M. Jose Morcillo, M. José Morcillo, M.Jose MORCILLO, M.José Morcillo, Ma José Morcillo, Ma. Jose Morcillo

45

Publications

684

Citations

14

H-Index

14

Concepts

All Affiliations

Universidad Nacional de Educación a DistanciaUniversidad Complutense de MadridUniversitat Autònoma de BarcelonaHospital Universitario Ramón y CajalUniversidad de Navarra
MJ

About

M. J. MORCILLO is an author at Universidad Nacional de Educación a Distancia specializing in pharmacology, chemistry, and natural sciences.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

6

6

145

2

Natural Sciences

6

6

148

3

Chemistry

6

6

130

4

Biochemistry

5

5

137

5

Engineering

1

1

19

M. J. MORCILLO

×

17

Publications

615

Citations

14

H-Index

YearCitations

Optimization of the Pharmacophore Model for 5-HT<sub>7</sub>R Antagonism. Design and Synthesis of New Naphtholactam and Naphthosultam Derivatives

María L. López-Rodrı́guez, Esther Porras, M. J. MORCILLO,

Journal of Medicinal Chemistry

2003

70

Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 2. Three-Dimensional Quantitative Structure−Activity Relationships of Hydantoin−Phenylpiperazine Derivatives with Affinity for 5-HT<sub>1A</sub> and α<sub>1</sub> Receptors. A Comparison of CoMFA Models

María L. López-Rodrı́guez, M. Luisa Rosado, Bellinda Benhamú,

Journal of Medicinal Chemistry

1997

64

Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 1. 2-[[4-(<i>o</i>-Methoxyphenyl)piperazin-1-yl]methyl]-1,3- dioxoperhydroimidazo[1,5-<i>a</i>]pyridine:  A Selective 5-HT<sub>1A</sub> Receptor Agonist

María L. López-Rodrı́guez, M. Luisa Rosado, Bellinda Benhamú,

Journal of Medicinal Chemistry

1996

63

Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 6. Study of the 5-HT<sub>1A</sub>/α<sub>1</sub>-Adrenergic Receptor Affinity by Classical Hansch Analysis, Artificial Neural Networks, and Computational Simulation of Ligand Recognition

María L. López-Rodrı́guez, M. J. MORCILLO, Esther Fernández,

Journal of Medicinal Chemistry

2000

56

Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 4. 1-[ω-(4-Arylpiperazin-1-yl)alkyl]-3-(diphenylmethylene)- 2,5-pyrrolidinediones and -3-(9<i>H</i>-fluoren-9-ylidene)-2,5-pyrrolidinediones: Study of the Steric Requirements of the Terminal Amide Fragment on 5-HT<sub>1A</sub> Affinity/Selectivity

María L. López-Rodrı́guez, M. J. MORCILLO, Tandú K. Rovat,

Journal of Medicinal Chemistry

1998

56

Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 5. Study of the Physicochemical Influence of the Pharmacophore on 5-HT<sub>1A</sub>/α<sub>1</sub>-Adrenergic Receptor Affinity:  Synthesis of a New Derivative with Mixed 5-HT<sub>1A</sub>/D<sub>2</sub> Antagonist Properties

María L. López-Rodrı́guez, M. J. MORCILLO, Esther Fernández,

Journal of Medicinal Chemistry

2000

54

Design, Synthesis and Pharmacological Evaluation of 5-Hydroxytryptamine1a Receptor Ligands to Explore the Three-Dimensional Structure of the Receptor

María L. López-Rodrı́guez, Bruno Vicente, Xavier Deupí,

Molecular Pharmacology

2002

46

Benzimidazole Derivatives. 2. Synthesis and Structure−Activity Relationships of New Azabicyclic Benzimidazole-4-carboxylic Acid Derivatives with Affinity for Serotoninergic 5-HT<sub>3</sub> Receptors

María L. López-Rodrı́guez, Bellinda Benhamú, M. J. MORCILLO,

Journal of Medicinal Chemistry

1999

42

Benzimidazole derivatives. Part 1: Synthesis and structure–activity relationships of new benzimidazole-4-carboxamides and carboxylates as potent and selective 5-HT4 receptor antagonists

María L. López-Rodrı́guez, Bellinda Benhamú, Alma Viso,

Bioorganic & Medicinal Chemistry

1999

34

Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 3. 2-[ω-(4-Arylpiperazin-1-yl)alkyl]perhydropyrrolo- [1,2-<i>c</i>]imidazoles and -perhydroimidazo[1,5-<i>a</i>]pyridines:  Study of the Influence of the Terminal Amide Fragment on 5-HT<sub>1A</sub>Affinity/Selectivity

María L. López-Rodrı́guez, M. J. MORCILLO, Esther Fernández,

Journal of Medicinal Chemistry

1997

32

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