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-Structure paper
Title | Structure-based design of 2-aminopyridine oxazolidinones as potent and selective tankyrase inhibitors. |
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Journal, issue, pages | ACS Med Chem Lett, Vol. 4, Page 1218-1223, Year 2013 |
Publish date | Oct 7, 2013 (structure data deposition date) |
Authors | Huang, H. / Guzman-Perez, A. / Acquaviva, L. / Berry, V. / Bregman, H. / Dovey, J. / Gunaydin, H. / Huang, X. / Huang, L. / Saffran, D. ...Huang, H. / Guzman-Perez, A. / Acquaviva, L. / Berry, V. / Bregman, H. / Dovey, J. / Gunaydin, H. / Huang, X. / Huang, L. / Saffran, D. / Serafino, R. / Schneider, S. / Wilson, C. / DiMauro, E.F. |
External links | ACS Med Chem Lett / PubMed:24900633 |
Methods | X-ray diffraction |
Resolution | 1.9 - 2.315 Å |
Structure data | PDB-4n3r: PDB-4n4t: PDB-4n4v: |
Chemicals | ChemComp-ZN: ChemComp-2GU: ChemComp-HOH: ChemComp-2GV: ChemComp-2GY: |
Source |
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Keywords | TRANSFERASE/TRANSFERASE INHIBITOR / tankyrase / PARP / inhibitor / TRANSFERASE-TRANSFERASE INHIBITOR complex |