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Title | 7-(Pyrazol-4-Yl)-3H-Imidazo[4,5-B]Pyridine-Based Derivatives for Kinase Inhibition: Co-Crystallisation Studies with Aurora-A Reveal Distinct Differences in the Orientation of the Pyrazole N1-Substituent. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 25, Page 4203-, Year 2015 |
Publish date | Jul 24, 2015 (structure data deposition date) |
Authors | Bavetsias, V. / Perez-Fuertes, Y. / Mcintyre, P.J. / Atrash, B. / Kosmopoulou, M. / O'Fee, L. / Burke, R. / Sun, C. / Faisal, A. / Bush, K. ...Bavetsias, V. / Perez-Fuertes, Y. / Mcintyre, P.J. / Atrash, B. / Kosmopoulou, M. / O'Fee, L. / Burke, R. / Sun, C. / Faisal, A. / Bush, K. / Avery, S. / Henley, A. / Raynaud, F.I. / Linardopoulos, S. / Bayliss, R. / Blagg, J. |
External links | Bioorg. Med. Chem. Lett. / PubMed:26296477 |
Methods | X-ray diffraction |
Resolution | 2.78 - 3.11 Å |
Structure data | PDB-5aad: PDB-5aae: PDB-5aaf: PDB-5aag: |
Chemicals | ChemComp-5GX: ChemComp-SO4: ChemComp-HOH: ChemComp-7HD: ChemComp-NL4: ChemComp-6F2: |
Source |
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Keywords | TRANSFERASE / AURORA-A / IMIDAZOPYRIDINE / AURORA KINASE / INHIBITOR |