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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


Research Triangle Park

North Carolina 27709



Name/email consistency: high



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


  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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