Discovery of benzoylisoindolines as a novel class of potent, selective and orally active GlyT1 inhibitors.
暂无分享,去创建一个
Markus Bender | Edilio Borroni | Daniela Alberati | Dominik Hainzl | Nicole Hauser | Emmanuel Pinard | Holger Fischer | E. Pinard | J. Moreau | E. Borroni | H. Fischer | Daniel Zimmerli | D. Hainzl | D. Alberati | Jean-Luc Moreau | R. Narquizian | S. Jolidon | Hans-Peter Marty | Daniel Zimmerli | M. Bender | Virginie Brom | Serge Burner | Remy Halm | Synèse Jolidon | Judith Lengyel | Thierry Meyer | Roland Mory | Robert Narquizian | Roger D Norcross | Philipp Schmid | Roger Wermuth | R. Norcross | P. Schmid | Nicole Hauser | R. Mory | Virginie Brom | S. Burner | R. Halm | Judith Lengyel | Hans-Peter Marty | Thierry Meyer | R. Wermuth
[1] Z. Rankovic,et al. Medicinal chemistry of hERG optimizations: Highlights and hang-ups. , 2006, Journal of medicinal chemistry.
[2] C. Parsons,et al. Glycine and N-methyl-D-aspartate receptors: physiological significance and possible therapeutic applications. , 1998, Pharmacological reviews.
[3] D. Javitt. Glycine transport inhibitors for the treatment of schizophrenia: symptom and disease modification. , 2009, Current opinion in drug discovery & development.
[4] E. Pinard,et al. Discovery of benzoylpiperazines as a novel class of potent and selective GlyT1 inhibitors. , 2008, Bioorganic & medicinal chemistry letters.
[5] Alexander Alanine,et al. 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. , 2010, Journal of medicinal chemistry.
[6] C. Sur,et al. Glycine transporter 1 inhibitors and modulation of NMDA receptor-mediated excitatory neurotransmission. , 2007, Current drug targets.
[7] Y. Shim,et al. A Convenient Preparation of Halide-Containing Quinolinic and Cinchomeronic Acid , 2002 .
[8] C. Lindsley,et al. Progress in the preparation and testing of glycine transporter type-1 (GlyT1) inhibitors. , 2006, Current topics in medicinal chemistry.
[9] C. Sur,et al. Recent progress in the discovery of non-sarcosine based GlyT1 inhibitors. , 2010, Current topics in medicinal chemistry.
[10] C. Christoffersen,et al. The synthesis and SAR of 2-arylsulfanyl-phenyl piperazinyl acetic acids as glyT-1 inhibitors. , 2004, Bioorganic & medicinal chemistry letters.
[11] Daniel C Javitt,et al. Glutamate and schizophrenia: phencyclidine, N-methyl-D-aspartate receptors, and dopamine-glutamate interactions. , 2007, International review of neurobiology.
[12] V. Ognyanov,et al. ALX 5407: a potent, selective inhibitor of the hGlyT1 glycine transporter. , 2001, Molecular pharmacology.
[13] K Gubernator,et al. Physicochemical high throughput screening: parallel artificial membrane permeation assay in the description of passive absorption processes. , 1998, Journal of medicinal chemistry.
[14] B. Kee,et al. Potentiation of the NMDA receptor in the treatment of schizophrenia: focused on the glycine site , 2007, European Archives of Psychiatry and Clinical Neuroscience.
[15] K. Hashimoto. Glycine Transport Inhibitors for the Treatment of Schizophrenia , 2010, The open medicinal chemistry journal.
[16] G. Walker,et al. Discovery and SAR of org 24598-a selective glycine uptake inhibitor. , 2001, Bioorganic & medicinal chemistry letters.
[17] P. Mátyus,et al. Glycine transporter type-1 and its inhibitors. , 2006, Current medicinal chemistry.