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-Structure paper
Title | 2,6-Naphthyridines as potent and selective inhibitors of the novel protein kinase C isozymes. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 21, Page 7367-7372, Year 2011 |
Publish date | Sep 23, 2011 (structure data deposition date) |
![]() | van Eis, M.J. / Evenou, J.P. / Floersheim, P. / Gaul, C. / Cowan-Jacob, S.W. / Monovich, L. / Rummel, G. / Schuler, W. / Stark, W. / Strauss, A. ...van Eis, M.J. / Evenou, J.P. / Floersheim, P. / Gaul, C. / Cowan-Jacob, S.W. / Monovich, L. / Rummel, G. / Schuler, W. / Stark, W. / Strauss, A. / Matt, A. / Vangrevelinghe, E. / Wagner, J. / Soldermann, N. |
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Methods | X-ray diffraction |
Resolution | 2.05 Å |
Structure data | ![]() PDB-3txo: |
Chemicals | ![]() ChemComp-07U: ![]() ChemComp-HOH: |
Source |
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![]() | TRANSFERASE/TRANSFERASE INHIBITOR / kinase / phosphotransferase / TRANSFERASE-TRANSFERASE INHIBITOR complex |