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-Structure paper
Title | Exploration of the 5-bromopyrimidin-4(3H)-ones as potent inhibitors of PDE5. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 23, Page 4944-4947, Year 2013 |
Publish date | Dec 5, 2012 (structure data deposition date) |
Authors | Gong, X. / Wang, G. / Ren, J. / Liu, Z. / Wang, Z. / Chen, T. / Yang, X. / Jiang, X. / Shen, J. / Jiang, H. ...Gong, X. / Wang, G. / Ren, J. / Liu, Z. / Wang, Z. / Chen, T. / Yang, X. / Jiang, X. / Shen, J. / Jiang, H. / Aisa, H.A. / Xu, Y. / Li, J. |
External links | Bioorg. Med. Chem. Lett. / PubMed:23867165 |
Methods | X-ray diffraction |
Resolution | 2.08 - 2.17 Å |
Structure data | PDB-4i9z: PDB-4ia0: |
Chemicals | ChemComp-5BA: ChemComp-ZN: ChemComp-MG: ChemComp-PEG: ChemComp-HOH: ChemComp-5BB: |
Source |
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Keywords | HYDROLASE/HYDROLASE INHIBITOR / HYDROLASE / HYDROLASE-HYDROLASE INHIBITOR complex |