15 articles for H Fischer
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Discovery of highly selective brain-penetrant vasopressin 1a antagonists for the potential treatment of autism via a chemogenomic and scaffold hopping approach.

F. Hoffmann-La Roche
3-Amido-3-aryl-piperidines: A Novel Class of Potent, Selective, and Orally Active GlyT1 Inhibitors.

F. Hoffmann-La Roche
ß-Secretase (BACE1) inhibitors with high in vivo efficacy suitable for clinical evaluation in Alzheimer's disease.

F. Hoffmann-La Roche
Cytotoxic effects of combination of oxidosqualene cyclase inhibitors with atorvastatin in human cancer cells.

Centre Hospitalier Universitaire Vaudois (Chuv) and University of Lausanne (Unil
Selective GlyT1 inhibitors: discovery of [4-(3-fluoro-5-trifluoromethylpyridin-2-yl)piperazin-1-yl][5-methanesulfonyl-2-((S)-2,2,2-trifluoro-1-methylethoxy)phenyl]methanone (RG1678), a promising novel medicine to treat schizophrenia.

F. Hoffmann-La Roche
Discovery of the imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepine scaffold as a novel, potent and selective GABA(A) alpha5 inverse agonist series.

F. Hoffmann-La Roche
Comparison of in vitro P-glycoprotein screening assays: recommendations for their use in drug discovery.

F. Hoffmann-La Roche
Discovery of benzoylisoindolines as a novel class of potent, selective and orally active GlyT1 inhibitors.

F. Hoffmann-La Roche
The discovery and unique pharmacological profile of RO4938581 and RO4882224 as potent and selective GABAA alpha5 inverse agonists for the treatment of cognitive dysfunction.

F. Hoffmann-La Roche
Imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepines as potent and highly selective GABAA alpha5 inverse agonists with potential for the treatment of cognitive dysfunction.

F. Hoffmann-La Roche
Aryl- and heteroaryl-substituted aminobenzo[a]quinolizines as dipeptidyl peptidase IV inhibitors.

F. Hoffmann-La Roche
Discovery of carmegliptin: a potent and long-acting dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes.

F. Hoffmann-La Roche
Design, synthesis and structure-activity relationship of simple bis-amides as potent inhibitors of GlyT1.

F. Hoffmann-La Roche
Discovery of benzoylpiperazines as a novel class of potent and selective GlyT1 inhibitors.

F. Hoffmann-La Roche
An aminomethylpyrimidine DPP-IV inhibitor with improved properties.

F. Hoffmann-La Roche