17 articles for S Rault
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Synthesis and characterization of a iodine-125-labeled pyrrolo[1,2-a]thieno[3,2-e]pyrazine and evaluation as a potential 5-HT4R SPECT tracer.

University of Caen Normandie
Novel and selective partial agonists of 5-HT3 receptors. 2. Synthesis and biological evaluation of piperazinopyridopyrrolopyrazines, piperazinopyrroloquinoxalines, and piperazinopyridopyrroloquinoxalines.

University of Caen Normandy
Novel selective and partial agonists of 5-HT3 receptors. Part 1. Synthesis and biological evaluation of piperazinopyrrolothienopyrazines.

University of Caen Normandy
First tricyclic oximino derivatives as 5-HT3 ligands.

University of Caen Normandy
Synthesis and structure-affinity relationships of selective high-affinity 5-HT(4) receptor antagonists: application to the design of new potential single photon emission computed tomography tracers.

University of Caen Normandie
New hypotheses for the binding mode of 4- and 7-substituted indazoles in the active site of neuronal nitric oxide synthase.

University of Caen Normandie
Novel antagonists of serotonin-4 receptors: synthesis and biological evaluation of pyrrolothienopyrazines.

Université
Synthesis of new dipyrrolo- and furopyrrolopyrazinones related to tripentones and their biological evaluation as potential kinases (CDKs1-5, GSK-3) inhibitors.

Université
Novel aminoethylbiphenyls as 5-HT7 receptor ligands.

Université
4-substituted indazoles as new inhibitors of neuronal nitric oxide synthase.

Upres-Ea 3915
Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands.

Université
New benzo[h][1,6]naphthyridine and azepino[3,2-c]quinoline derivatives as selective antagonists of 5-HT4 receptors: binding profile and pharmacological characterization.

Université
Inhibition of neuronal nitric oxide synthase by 7-methoxyindazole and related substituted indazoles.

Université
Design, synthesis, and evaluation of novel thienopyrrolizinones as antitubulin agents.

University of Caen Normandy
Tau protein aggregation in Alzheimer's disease: An attractive target for the development of novel therapeutic agents.

University of Caen Normandie
Molecular pharmacology of somatostatin receptors.

Sandoz Pharma
Carbonic anhydrase inhibitors. Inhibition and homology modeling studies of the fungal beta-carbonic anhydrase from Candida albicans with sulfonamides.

Universite Degli Studi Di Firenze