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-Structure paper
Title | Substituted 4-(Thiazol-5-Yl)-2-(Phenylamino)Pyrimidines are Highly Active Cdk9 Inhibitors: Synthesis, X-Ray Crystal Structure, Sar and Anti-Cancer Activities. |
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Journal, issue, pages | J. Med. Chem., Vol. 56, Page 640-, Year 2013 |
Publish date | Oct 2, 2012 (structure data deposition date) |
Authors | Shao, H. / Shi, S. / Huang, S. / Hole, A. / Abbas, A.Y. / Baumli, S. / Liu, X. / Lam, F. / Foley, D.W. / Fischer, P.M. ...Shao, H. / Shi, S. / Huang, S. / Hole, A. / Abbas, A.Y. / Baumli, S. / Liu, X. / Lam, F. / Foley, D.W. / Fischer, P.M. / Noble, M. / Endicott, J.A. / Pepper, C. / Wang, S. |
External links | J. Med. Chem. / PubMed:23301767 |
Methods | X-ray diffraction |
Resolution | 2.26 - 3.085 Å |
Structure data | PDB-4bcg: PDB-4bcp: |
Chemicals | ChemComp-T3C: ChemComp-GOL: ChemComp-HOH: ChemComp-SO4: ChemComp-SGM: |
Source |
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Keywords | TRANSFERASE/CELL CYCLE / TRANSFERASE-CELL CYCLE COMPLEX / CDK-CYCLIN COMPLEX / TRANSCRIPTION-PROTEIN BINDING / STRUCTURE-BASED DRUG DESIGN / CYCLIN-INHIBITOR |