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-Structure paper
Title | From PROTAC to inhibitor: Structure-guided discovery of potent and orally bioavailable BET inhibitors. |
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Journal, issue, pages | Eur. J. Med. Chem., Vol. 251, Page 115246-115246, Year 2023 |
Publish date | Jul 27, 2021 (structure data deposition date) |
Authors | Koravovic, M. / Mayasundari, A. / Tasic, G. / Keramatnia, F. / Stachowski, T.R. / Cui, H. / Chai, S.C. / Jonchere, B. / Yang, L. / Li, Y. ...Koravovic, M. / Mayasundari, A. / Tasic, G. / Keramatnia, F. / Stachowski, T.R. / Cui, H. / Chai, S.C. / Jonchere, B. / Yang, L. / Li, Y. / Fu, X. / Hiltenbrand, R. / Paul, L. / Mishra, V. / Klco, J.M. / Roussel, M.F. / Pomerantz, W.C. / Fischer, M. / Rankovic, Z. / Savic, V. |
External links | Eur. J. Med. Chem. / PubMed:36898329 |
Methods | X-ray diffraction |
Resolution | 1.05 - 1.18 Å |
Structure data | PDB-7rmd: PDB-7rn2: |
Chemicals | ChemComp-EDO: ChemComp-5Z0: ChemComp-HOH: ChemComp-5ZQ: |
Source |
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Keywords | CELL CYCLE / bromodomain-containing protein 4 isoform long / BRD4 / bromodomain containing protein 4 / mitotic chromosome associated protein |