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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Emmanuel Pinard

F. Hoffmann-La Roche Ltd

Pharmaceutical Research Basel

Discovery Chemistry

CH-4070 Basel

Switzerland

[email]@roche.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • F. Hoffmann-La Roche Ltd, Pharmaceutical Research Basel, Discovery Chemistry, CH-4070 Basel, Switzerland. 2006 - 2008
  • Pharma Division, Discovery Chemistry, F. Hoffmann-La Roche Ltd., CH-4070, Switzerland. 2001 - 2002

References

  1. Discovery of benzoylpiperazines as a novel class of potent and selective GlyT1 inhibitors. Pinard, E., Alberati, D., Borroni, E., Fischer, H., Hainzl, D., Jolidon, S., Moreau, J.L., Narquizian, R., Nettekoven, M., Norcross, R.D., Stalder, H., Thomas, A.W. Bioorg. Med. Chem. Lett. (2008) [Pubmed]
  2. Discovery of N-(2-aryl-cyclohexyl) substituted spiropiperidines as a novel class of GlyT1 inhibitors. Pinard, E., Ceccarelli, S.M., Stalder, H., Alberati, D. Bioorg. Med. Chem. Lett. (2006) [Pubmed]
  3. 4-Aminoquinolines as a novel class of NR1/2B subtype selective NMDA receptor antagonists. Pinard, E., Alanine, A., Bourson, A., Büttelmann, B., Heitz, M., Mutela Ramanjit Gill, V., Trube, G., Wyler, R. Bioorg. Med. Chem. Lett. (2002) [Pubmed]
  4. Discovery of (R)-1-[2-hydroxy-3-(4-hydroxy-phenyl)-propyl]-4-(4-methyl-benzyl)-piperidin-4-ol: a novel NR1/2B subtype selective NMDA receptor antagonist. Pinard, E., Alanine, A., Bourson, A., Büttelmann, B., Gill, R., Heitz, M., Jaeschke, G., Mutel, V., Trube, G., Wyler, R. Bioorg. Med. Chem. Lett. (2001) [Pubmed]
 
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