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-Structure paper
Title | Design, synthesis, and biological evaluation of pyrazolopyrimidine-sulfonamides as potent multiple-mitotic kinase (MMK) inhibitors (part I). |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 21, Page 5633-5637, Year 2011 |
Publish date | Mar 11, 2011 (structure data deposition date) |
Authors | Zhang, L. / Fan, J. / Chong, J.H. / Cesena, A. / Tam, B.Y. / Gilson, C. / Boykin, C. / Wang, D. / Aivazian, D. / Marcotte, D. ...Zhang, L. / Fan, J. / Chong, J.H. / Cesena, A. / Tam, B.Y. / Gilson, C. / Boykin, C. / Wang, D. / Aivazian, D. / Marcotte, D. / Xiao, G. / Le Brazidec, J.Y. / Piao, J. / Lundgren, K. / Hong, K. / Vu, K. / Nguyen, K. / Gan, L.S. / Silvian, L. / Ling, L. / Teng, M. / Reff, M. / Takeda, N. / Timple, N. / Wang, Q. / Morena, R. / Khan, S. / Zhao, S. / Li, T. / Lee, W.C. / Taveras, A.G. / Chao, J. |
External links | Bioorg. Med. Chem. Lett. / PubMed:21798738 |
Methods | X-ray diffraction |
Resolution | 2.9 Å |
Structure data | PDB-3r21: PDB-3r22: |
Chemicals | ChemComp-D36: ChemComp-MG: ChemComp-D37: ChemComp-HOH: |
Source |
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Keywords | transferase/transferase inhibitor / Kinase domain / transferase-transferase inhibitor complex |