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Title | Discovery of novel, induced-pocket binding oxazolidinones as potent, selective, and orally bioavailable tankyrase inhibitors. |
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Journal, issue, pages | J. Med. Chem., Vol. 56, Page 4320-4342, Year 2013 |
Publish date | Apr 12, 2013 (structure data deposition date) |
Authors | Bregman, H. / Chakka, N. / Guzman-Perez, A. / Gunaydin, H. / Gu, Y. / Huang, X. / Berry, V. / Liu, J. / Teffera, Y. / Huang, L. ...Bregman, H. / Chakka, N. / Guzman-Perez, A. / Gunaydin, H. / Gu, Y. / Huang, X. / Berry, V. / Liu, J. / Teffera, Y. / Huang, L. / Egge, B. / Mullady, E.L. / Schneider, S. / Andrews, P.S. / Mishra, A. / Newcomb, J. / Serafino, R. / Strathdee, C.A. / Turci, S.M. / Wilson, C. / Dimauro, E.F. |
External links | J. Med. Chem. / PubMed:23701517 |
Methods | X-ray diffraction |
Resolution | 2.3 - 2.9 Å |
Structure data | PDB-4k4e: PDB-4k4f: |
Chemicals | ChemComp-ZN: ChemComp-K4E: ChemComp-HOH: ChemComp-K4F: |
Source |
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Keywords | Transferase/Transferase Inhibitor / PARP / Transferase-Transferase Inhibitor complex |