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-Structure paper
Title | Discovery of 3-(3-(4-(1-Aminocyclobutyl)phenyl)-5-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amine (ARQ 092): An Orally Bioavailable, Selective, and Potent Allosteric AKT Inhibitor. |
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Journal, issue, pages | J. Med. Chem., Vol. 59, Page 6455-6469, Year 2016 |
Publish date | Jun 7, 2016 (structure data deposition date) |
![]() | Lapierre, J.M. / Eathiraj, S. / Vensel, D. / Liu, Y. / Bull, C.O. / Cornell-Kennon, S. / Iimura, S. / Kelleher, E.W. / Kizer, D.E. / Koerner, S. ...Lapierre, J.M. / Eathiraj, S. / Vensel, D. / Liu, Y. / Bull, C.O. / Cornell-Kennon, S. / Iimura, S. / Kelleher, E.W. / Kizer, D.E. / Koerner, S. / Makhija, S. / Matsuda, A. / Moussa, M. / Namdev, N. / Savage, R.E. / Szwaya, J. / Volckova, E. / Westlund, N. / Wu, H. / Schwartz, B. |
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Methods | X-ray diffraction |
Resolution | 2.7 Å |
Structure data | ![]() PDB-5kcv: |
Chemicals | ![]() ChemComp-6S1: ![]() ChemComp-HOH: |
Source |
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![]() | TRANSFERASE/INHIBITOR / AKT / Allosteric inhibitor / Kinase inhibitor / TRANSFERASE-INHIBITOR complex |