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Title | Identification of C-2 Hydroxyethyl Imidazopyrrolopyridines as Potent JAK1 Inhibitors with Favorable Physicochemical Properties and High Selectivity over JAK2. |
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Journal, issue, pages | J. Med. Chem., Vol. 56, Page 4764-4785, Year 2013 |
Publish date | Jan 22, 2013 (structure data deposition date) |
Authors | Zak, M. / Hurley, C.A. / Ward, S.I. / Bergeron, P. / Barrett, K. / Balazs, M. / Blair, W.S. / Bull, R. / Chakravarty, P. / Chang, C. ...Zak, M. / Hurley, C.A. / Ward, S.I. / Bergeron, P. / Barrett, K. / Balazs, M. / Blair, W.S. / Bull, R. / Chakravarty, P. / Chang, C. / Crackett, P. / Deshmukh, G. / Devoss, J. / Dragovich, P.S. / Eigenbrot, C. / Ellwood, C. / Gaines, S. / Ghilardi, N. / Gibbons, P. / Gradl, S. / Gribling, P. / Hamman, C. / Harstad, E. / Hewitt, P. / Johnson, A. / Johnson, T. / Kenny, J.R. / Koehler, M.F. / Bir Kohli, P. / Labadie, S. / Lee, W.P. / Liao, J. / Liimatta, M. / Mendonca, R. / Narukulla, R. / Pulk, R. / Reeve, A. / Savage, S. / Shia, S. / Steffek, M. / Ubhayakar, S. / van Abbema, A. / Aliagas, I. / Avitabile-Woo, B. / Xiao, Y. / Yang, J. / Kulagowski, J.J. |
External links | J. Med. Chem. / PubMed:23659214 |
Methods | X-ray diffraction |
Resolution | 1.5 - 2.35 Å |
Structure data | PDB-4iva: PDB-4ivb: PDB-4ivc: PDB-4ivd: |
Chemicals | ChemComp-1J5: ChemComp-HOH: ChemComp-1J6: ChemComp-15T: |
Source |
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Keywords | TRANSFERASE/TRANSFERASE INHIBITOR / PROTEIN KINASE / PHOSPHOTRANSFER / TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX / PHOSPHO TRANSFER / PHOSPHO TYROSINE / TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX |