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-Structure paper
Title | Discovery of Aryl Aminoquinazoline Pyridones as Potent, Selective, and Orally Efficacious Inhibitors of Receptor Tyrosine Kinase c-Kit. |
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Journal, issue, pages | J. Med. Chem., Vol. 51, Page 3065-3068, Year 2008 |
Publish date | Mar 31, 2008 (structure data deposition date) |
Authors | Hu, E. / Tasker, A. / White, R.D. / Kunz, R.K. / Human, J. / Chen, N. / Burli, R. / Hungate, R. / Novak, P. / Itano, A. ...Hu, E. / Tasker, A. / White, R.D. / Kunz, R.K. / Human, J. / Chen, N. / Burli, R. / Hungate, R. / Novak, P. / Itano, A. / Zhang, X. / Yu, V. / Nguyen, Y. / Tudor, Y. / Plant, M. / Flynn, S. / Xu, Y. / Meagher, K.L. / Whittington, D.A. / Ng, G.Y. |
External links | J. Med. Chem. / PubMed:18447379 |
Methods | X-ray diffraction |
Resolution | 2.4 - 2.7 Å |
Structure data | PDB-3cp9: PDB-3cpb: PDB-3cpc: |
Chemicals | ChemComp-C19: ChemComp-HOH: ChemComp-C92: ChemComp-C52: |
Source |
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Keywords | TRANSFERASE / receptor tyrosine kinase / angiogenesis / ATP-binding / Developmental protein / Differentiation / Glycoprotein / Host-virus interaction / Immunoglobulin domain / Membrane / Nucleotide-binding / Phosphoprotein / Polymorphism / Transmembrane / Tyrosine-protein kinase |