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| Title | 6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors. |
|---|---|
| Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 20, Page 4350-4354, Year 2010 |
| Publish date | May 21, 2010 (structure data deposition date) |
 Authors | Cai, J. / Baugh, M. / Black, D. / Long, C. / Jonathan Bennett, D. / Dempster, M. / Fradera, X. / Gillespie, J. / Andrews, F. / Boucharens, S. ...Cai, J. / Baugh, M. / Black, D. / Long, C. / Jonathan Bennett, D. / Dempster, M. / Fradera, X. / Gillespie, J. / Andrews, F. / Boucharens, S. / Bruin, J. / Cameron, K.S. / Cumming, I. / Hamilton, W. / Jones, P.S. / Kaptein, A. / Kinghorn, E. / Maidment, M. / Martin, I. / Mitchell, A. / Rankovic, Z. / Robinson, J. / Scullion, P. / Uitdehaag, J.C. / Vink, P. / Westwood, P. / van Zeeland, M. / van Berkom, L. / Bastiani, M. / Meulemans, T. |
 External links | Bioorg. Med. Chem. Lett. / PubMed:20598883 |
| Methods | X-ray diffraction |
| Resolution | 1.9 Å |
| Structure data |  PDB-3n4c: |
| Chemicals |  ChemComp-EF3:  ChemComp-DMS:  ChemComp-SO4:  ChemComp-HOH: |
| Source |
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 Keywords | HYDROLASE/HYDROLASE INHIBITOR / Cathepsin S / covalent inhibitor / HYDROLASE / HYDROLASE-HYDROLASE INHIBITOR complex |
homo sapiens (human)