PMID

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Article Title

Organization

Synthesis and antidopaminergic activity of some 3-(aminomethyl)tetralones as analogues of butyrophenone.

University of Santiago De Compostela

Selective and potent adenosine A3 receptor antagonists by methoxyaryl substitution on the N-(2,6-diarylpyrimidin-4-yl)acetamide scaffold.

University of Santiago De Compostela

2D MI-DRAGON: a new predictor for protein-ligands interactions and theoretic-experimental studies of US FDA drug-target network, oxoisoaporphine inhibitors for MAO-A and human parasite proteins.

University of Santiago De Compostela

Synthesis and study of a series of 3-arylcoumarins as potent and selective monoamine oxidase B inhibitors.

University of Santiago De Compostela

Aromatic ring functionalization of benzolactam derivatives: new potent dopamine D3 receptor ligands.

University of Santiago De Compostela

Pyrimidine derivatives as potent and selective A3 adenosine receptor antagonists.

University of Santiago De Compostela

Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.

University of Santiago De Compostela

Further Studies on the Highly Active Des-C-Ring and Aromatic-D-Ring Analogues of 1α,25-Dihydroxyvitamin D

University of Santiago De Compostela

Exploring the Effect of Halogenation in a Series of Potent and Selective A

University of Santiago de Compostela

A QSAR model for in silico screening of MAO-A inhibitors. Prediction, synthesis, and biological assay of novel coumarins.

University of Santiago De Compostela

Design, Synthesis, Biological Activity, and Structural Analysis of Novel Des-C-Ring and Aromatic-D-Ring Analogues of 1α,25-Dihydroxyvitamin D

University of Santiago De Compostela

Discovery of 3,4-Dihydropyrimidin-2(1H)-ones As a Novel Class of Potent and Selective A2B Adenosine Receptor Antagonists.

University of Santiago De Compostela

Novel (coumarin-3-yl)carbamates as selective MAO-B inhibitors: synthesis, in vitro and in vivo assays, theoretical evaluation of ADME properties and docking study.

University of Santiago De Compostela

Synthesis, adenosine receptor binding and 3D-QSAR of 4-substituted 2-(2'-furyl)-1,2,4-triazolo[1,5-a]quinoxalines.

University of Santiago De Compostela

Synthesis and atypical antipsychotic profile of some 2-(2-piperidinoethyl)benzocycloalkanones as analogues of butyrophenone.

University of Santiago De Compostela

Aromatic-Based Design of Highly Active and Noncalcemic Vitamin D Receptor Agonists.

University of Santiago De Compostela