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17 articles for S Rault


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
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.EBI
University of Caen Normandie
Novel and selective partial agonists of 5-HT3 receptors. 2. Synthesis and biological evaluation of piperazinopyridopyrrolopyrazines, piperazinopyrroloquinoxalines, and piperazinopyridopyrroloquinoxalines.EBI
University of Caen Normandy
Novel selective and partial agonists of 5-HT3 receptors. Part 1. Synthesis and biological evaluation of piperazinopyrrolothienopyrazines.EBI
University of Caen Normandy
First tricyclic oximino derivatives as 5-HT3 ligands.EBI
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.EBI
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.EBI
University of Caen Normandie
Novel antagonists of serotonin-4 receptors: synthesis and biological evaluation of pyrrolothienopyrazines.EBI
Université
Synthesis of new dipyrrolo- and furopyrrolopyrazinones related to tripentones and their biological evaluation as potential kinases (CDKs1-5, GSK-3) inhibitors.EBI
Université
Novel aminoethylbiphenyls as 5-HT7 receptor ligands.EBI
Université
4-substituted indazoles as new inhibitors of neuronal nitric oxide synthase.EBI
Upres-Ea 3915
Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands.EBI
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.EBI
Université
Inhibition of neuronal nitric oxide synthase by 7-methoxyindazole and related substituted indazoles.EBI
Université
Design, synthesis, and evaluation of novel thienopyrrolizinones as antitubulin agents.EBI
University of Caen Normandy
Tau protein aggregation in Alzheimer's disease: An attractive target for the development of novel therapeutic agents.EBI
University of Caen Normandie
Molecular pharmacology of somatostatin receptors.BDB
Sandoz Pharma
Carbonic anhydrase inhibitors. Inhibition and homology modeling studies of the fungal beta-carbonic anhydrase from Candida albicans with sulfonamides.BDB
Universite Degli Studi Di Firenze