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Title | Structure-Based Optimization of Potent, Selective, and Orally Bioavailable CDK8 Inhibitors Discovered by High-Throughput Screening. |
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Journal, issue, pages | J. Med. Chem., Vol. 59, Page 9337-9349, Year 2016 |
Publish date | Feb 23, 2016 (structure data deposition date) |
![]() | Czodrowski, P. / Mallinger, A. / Wienke, D. / Esdar, C. / Poschke, O. / Busch, M. / Rohdich, F. / Eccles, S.A. / Ortiz-Ruiz, M.J. / Schneider, R. ...Czodrowski, P. / Mallinger, A. / Wienke, D. / Esdar, C. / Poschke, O. / Busch, M. / Rohdich, F. / Eccles, S.A. / Ortiz-Ruiz, M.J. / Schneider, R. / Raynaud, F.I. / Clarke, P.A. / Musil, D. / Schwarz, D. / Dale, T. / Urbahns, K. / Blagg, J. / Schiemann, K. |
![]() | ![]() ![]() |
Methods | X-ray diffraction |
Resolution | 2.18 - 2.65 Å |
Structure data | ![]() PDB-5icp: ![]() PDB-5idn: ![]() PDB-5idp: |
Chemicals | ![]() ChemComp-69Z: ![]() ChemComp-EDO: ![]() ChemComp-FMT: ![]() ChemComp-HOH: ![]() ChemComp-6A7: ![]() ChemComp-6A6: |
Source |
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![]() | TRANSFERASE / CDK8 KINASE / CYCLIN C |