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-Structure paper
Title | Development of o-Chlorophenyl Substituted Pyrimidines as Exceptionally Potent Aurora Kinase Inhibitors. |
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Journal, issue, pages | J. Med. Chem., Vol. 55, Page 7392-7416, Year 2012 |
Publish date | Nov 17, 2011 (structure data deposition date) |
Authors | Lawrence, H.R. / Martin, M.P. / Luo, Y. / Pireddu, R. / Yang, H. / Gevariya, H. / Ozcan, S. / Zhu, J.Y. / Kendig, R. / Rodriguez, M. ...Lawrence, H.R. / Martin, M.P. / Luo, Y. / Pireddu, R. / Yang, H. / Gevariya, H. / Ozcan, S. / Zhu, J.Y. / Kendig, R. / Rodriguez, M. / Elias, R. / Cheng, J.Q. / Sebti, S.M. / Schonbrunn, E. / Lawrence, N.J. |
External links | J. Med. Chem. / PubMed:22803810 |
Methods | X-ray diffraction |
Resolution | 2.3 - 3.05 Å |
Structure data | PDB-3up7: PDB-4dea: PDB-4deb: PDB-4ded: PDB-4dee: |
Chemicals | ChemComp-0C9: ChemComp-HOH: ChemComp-EDO: ChemComp-NHI: ChemComp-NHJ: ChemComp-NHU: ChemComp-MG: ChemComp-ADP: |
Source |
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Keywords | TRANSFERASE/TRANSFERASE INHIBITOR / protein kinase / Aurora A / inhibitor / DFG-in / TRANSFERASE-TRANSFERASE INHIBITOR complex / TRANSFERASE |