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

Francis X. Tavares

Department of Medicinal Chemistry

GlaxoSmithKline

Research Triangle Park

North Carolina 27709

USA

[email]@gsk.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medicinal Chemistry, GlaxoSmithKline, Research Triangle Park, North Carolina 27709, USA. 2004 - 2006

References

  1. 6-(4-chlorophenyl)-3-substituted-thieno[3,2-d]pyrimidin-4(3H)-one-based melanin-concentrating hormone receptor 1 antagonist. Tavares, F.X., Al-Barazanji, K.A., Bishop, M.J., Britt, C.S., Carlton, D.L., Cooper, J.P., Feldman, P.L., Garrido, D.M., Goetz, A.S., Grizzle, M.K., Hertzog, D.L., Ignar, D.M., Lang, D.G., McIntyre, M.S., Ott, R.J., Peat, A.J., Zhou, H.Q. J. Med. Chem. (2006) [Pubmed]
  2. Potent, selective, and orally efficacious antagonists of melanin-concentrating hormone receptor 1. Tavares, F.X., Al-Barazanji, K.A., Bigham, E.C., Bishop, M.J., Britt, C.S., Carlton, D.L., Feldman, P.L., Goetz, A.S., Grizzle, M.K., Guo, Y.C., Handlon, A.L., Hertzog, D.L., Ignar, D.M., Lang, D.G., Ott, R.J., Peat, A.J., Zhou, H.Q. J. Med. Chem. (2006) [Pubmed]
  3. Design of potent, selective, and orally bioavailable inhibitors of cysteine protease cathepsin k. Tavares, F.X., Boncek, V., Deaton, D.N., Hassell, A.M., Long, S.T., Miller, A.B., Payne, A.A., Miller, L.R., Shewchuk, L.M., Wells-Knecht, K., Willard, D.H., Wright, L.L., Zhou, H.Q. J. Med. Chem. (2004) [Pubmed]
  4. N-Phenyl-4-pyrazolo[1,5-b]pyridazin-3-ylpyrimidin-2-amines as potent and selective inhibitors of glycogen synthase kinase 3 with good cellular efficacy. Tavares, F.X., Boucheron, J.A., Dickerson, S.H., Griffin, R.J., Preugschat, F., Thomson, S.A., Wang, T.Y., Zhou, H.Q. J. Med. Chem. (2004) [Pubmed]
 
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