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-Structure paper
Title | Achieving multi-isoform PI3K inhibition in a series of substituted 3,4-dihydro-2H-benzo[1,4]oxazines |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 18, Page 4700-4704, Year 2008 |
Publish date | Jul 8, 2008 (structure data deposition date) |
Authors | Perry, B. / Alexander, R. / Bennett, G. / Buckley, G. / Ceska, T. / Crabbe, T. / Dale, V. / Gowers, L. / Horsley, H. / James, L. ...Perry, B. / Alexander, R. / Bennett, G. / Buckley, G. / Ceska, T. / Crabbe, T. / Dale, V. / Gowers, L. / Horsley, H. / James, L. / Jenkins, K. / Crepy, K. / Kulisa, C. / Lightfoot, H. / Lock, C. / Mack, S. / Morgan, T. / Nicolas, A.-L. / Pitt, W. / Sabin, V. / Wright, S. |
External links | Bioorg. Med. Chem. Lett. / PubMed:18644721 |
Methods | X-ray diffraction |
Resolution | 2.85 Å |
Structure data | PDB-3dpd: |
Chemicals | ChemComp-41A: |
Source |
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Keywords | TRANSFERASE / PHOSPHOINOSITIDE 3-KINASE GAMMA / SECONDARY MESSENGER GENERATION / PI3K / PI 3K / Kinase |