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-Structure paper
Title | Discovery of potent, selective and orally bioavailable imidazo[1,5-a]pyrazine derived ACK1 inhibitors. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 23, Page 979-984, Year 2013 |
Publish date | Dec 11, 2012 (structure data deposition date) |
![]() | Jin, M. / Wang, J. / Kleinberg, A. / Kadalbajoo, M. / Siu, K.W. / Cooke, A. / Bittner, M.A. / Yao, Y. / Thelemann, A. / Ji, Q. ...Jin, M. / Wang, J. / Kleinberg, A. / Kadalbajoo, M. / Siu, K.W. / Cooke, A. / Bittner, M.A. / Yao, Y. / Thelemann, A. / Ji, Q. / Bhagwat, S. / Mulvihill, K.M. / Rechka, J.A. / Pachter, J.A. / Crew, A.P. / Epstein, D. / Mulvihill, M.J. |
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Methods | X-ray diffraction |
Resolution | 3 Å |
Structure data | ![]() PDB-4id7: |
Chemicals | ![]() ChemComp-1G0: ![]() ChemComp-SO4: ![]() ChemComp-HOH: |
Source |
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![]() | TRANSFERASE/TRANSFERASE INHIBITOR / Kinase / TRANSFERASE-TRANSFERASE INHIBITOR complex |