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Gee-Hong Kuo

Drug Discovery Division

Johnson and Johnson Pharmaceutical Research and Development

L.L.C.

1000 Route 202

USA

[email]@prdus.jnj.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Drug Discovery Division, Johnson and Johnson Pharmaceutical Research and Development, L.L.C., 1000 Route 202, USA. 2003 - 2005

References

  1. Synthesis and discovery of pyrazine-pyridine biheteroaryl as a novel series of potent vascular endothelial growth factor receptor-2 inhibitors. Kuo, G.H., Wang, A., Emanuel, S., Deangelis, A., Zhang, R., Connolly, P.J., Murray, W.V., Gruninger, R.H., Sechler, J., Fuentes-Pesquera, A., Johnson, D., Middleton, S.A., Jolliffe, L., Chen, X. J. Med. Chem. (2005) [Pubmed]
  2. Synthesis and identification of [1,3,5]triazine-pyridine biheteroaryl as a novel series of potent cyclin-dependent kinase inhibitors. Kuo, G.H., Deangelis, A., Emanuel, S., Wang, A., Zhang, Y., Connolly, P.J., Chen, X., Gruninger, R.H., Rugg, C., Fuentes-Pesquera, A., Middleton, S.A., Jolliffe, L., Murray, W.V. J. Med. Chem. (2005) [Pubmed]
  3. Synthesis and structure-activity relationships of pyrazine-pyridine biheteroaryls as novel, potent, and selective vascular endothelial growth factor receptor-2 inhibitors. Kuo, G.H., Prouty, C., Wang, A., Emanuel, S., Deangelis, A., Zhang, Y., Song, F., Beall, L., Connolly, P.J., Karnachi, P., Chen, X., Gruninger, R.H., Sechler, J., Fuentes-Pesquera, A., Middleton, S.A., Jolliffe, L., Murray, W.V. J. Med. Chem. (2005) [Pubmed]
  4. Synthesis and discovery of macrocyclic polyoxygenated bis-7-azaindolylmaleimides as a novel series of potent and highly selective glycogen synthase kinase-3beta inhibitors. Kuo, G.H., Prouty, C., DeAngelis, A., Shen, L., O'Neill, D.J., Shah, C., Connolly, P.J., Murray, W.V., Conway, B.R., Cheung, P., Westover, L., Xu, J.Z., Look, R.A., Demarest, K.T., Emanuel, S., Middleton, S.A., Jolliffe, L., Beavers, M.P., Chen, X. J. Med. Chem. (2003) [Pubmed]
 
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