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-Structure paper
Title | Pyrazolopyridines as potent PDE4B inhibitors: 5-heterocycle SAR. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 20, Page 5803-5806, Year 2010 |
Publish date | Jul 28, 2010 (structure data deposition date) |
Authors | Mitchell, C.J. / Ballantine, S.P. / Coe, D.M. / Cook, C.M. / Delves, C.J. / Dowle, M.D. / Edlin, C.D. / Hamblin, J.N. / Holman, S. / Johnson, M.R. ...Mitchell, C.J. / Ballantine, S.P. / Coe, D.M. / Cook, C.M. / Delves, C.J. / Dowle, M.D. / Edlin, C.D. / Hamblin, J.N. / Holman, S. / Johnson, M.R. / Jones, P.S. / Keeling, S.E. / Kranz, M. / Lindvall, M. / Lucas, F.S. / Neu, M. / Solanke, Y.E. / Somers, D.O. / Trivedi, N.A. / Wiseman, J.O. |
External links | Bioorg. Med. Chem. Lett. / PubMed:20732811 |
Methods | X-ray diffraction |
Resolution | 2 - 2.42 Å |
Structure data | PDB-3o56: PDB-3o57: |
Chemicals | ChemComp-ZN: ChemComp-MG: ChemComp-ARS: ChemComp-ZG1: ChemComp-GOL: ChemComp-HOH: ChemComp-ZG2: |
Source |
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Keywords | HYDROLASE/HYDROLASE INHIBITOR / PDE / HYDROLASE / PHOSPHODIESTERASE / cAMP Binding / HYDROLASE-HYDROLASE INHIBITOR complex |