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-Structure paper
Title | Hit-to-lead optimization and kinase selectivity of imidazo[1,2-a]quinoxalin-4-amine derived JNK1 inhibitors. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 23, Page 5217-5222, Year 2013 |
Publish date | Jun 13, 2013 (structure data deposition date) |
Authors | Li, B. / Cociorva, O.M. / Nomanbhoy, T. / Weissig, H. / Li, Q. / Nakamura, K. / Liyanage, M. / Zhang, M.C. / Shih, A.Y. / Aban, A. ...Li, B. / Cociorva, O.M. / Nomanbhoy, T. / Weissig, H. / Li, Q. / Nakamura, K. / Liyanage, M. / Zhang, M.C. / Shih, A.Y. / Aban, A. / Hu, Y. / Cajica, J. / Pham, L. / Kozarich, J.W. / Shreder, K.R. |
External links | Bioorg. Med. Chem. Lett. / PubMed:23916259 |
Methods | X-ray diffraction |
Resolution | 1.95 Å |
Structure data | PDB-4l7f: |
Chemicals | ChemComp-1V5: ChemComp-HOH: |
Source |
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Keywords | Transferase/Transferase Inhibitor / protein kinase fold / protein kinase / jun-c / phosphorylation / Transferase-Transferase Inhibitor complex |