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-Structure paper
Title | Development of Selective Pyrido[2,3- d ]pyrimidin-7(8 H )-one-Based Mammalian STE20-Like (MST3/4) Kinase Inhibitors. |
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Journal, issue, pages | J. Med. Chem., Vol. 67, Page 3813-3842, Year 2024 |
Publish date | Dec 14, 2022 (structure data deposition date) |
Authors | Rak, M. / Menge, A. / Tesch, R. / Berger, L.M. / Balourdas, D.I. / Shevchenko, E. / Kramer, A. / Elson, L. / Berger, B.T. / Abdi, I. ...Rak, M. / Menge, A. / Tesch, R. / Berger, L.M. / Balourdas, D.I. / Shevchenko, E. / Kramer, A. / Elson, L. / Berger, B.T. / Abdi, I. / Wahl, L.M. / Poso, A. / Kaiser, A. / Hanke, T. / Kronenberger, T. / Joerger, A.C. / Muller, S. / Knapp, S. |
External links | J. Med. Chem. / PubMed:38422480 |
Methods | X-ray diffraction |
Resolution | 1.47 - 2.52 Å |
Structure data | PDB-8bzj: PDB-8qlr: PDB-8qls: PDB-8qlt: |
Chemicals | ChemComp-SJX: ChemComp-EDO: ChemComp-HOH: ChemComp-VYN: ChemComp-VYH: ChemComp-VZ2: |
Source |
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Keywords | TRANSFERASE / selective kinase inhibitors / structure-based drug design / structure-guided drug design |