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| Title | Discovery of Aryl Aminoquinazoline Pyridones as Potent, Selective, and Orally Efficacious Inhibitors of Receptor Tyrosine Kinase c-Kit. |
|---|---|
| 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 |
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homo sapiens (human)
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