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TitleSynthesis and SAR of aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitors
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 17, Page 3463-3467, Year 2007
Publish dateMar 8, 2007 (structure data deposition date)
AuthorsAlam, M. / Beevers, R.E. / Ceska, T. / Davenport, R.J. / Dickson, K.M. / Fortunato, M. / Gowers, L. / Haughan, A.F. / James, L.A. / Jones, M.W. ...Alam, M. / Beevers, R.E. / Ceska, T. / Davenport, R.J. / Dickson, K.M. / Fortunato, M. / Gowers, L. / Haughan, A.F. / James, L.A. / Jones, M.W. / Kinsella, N. / Lowe, C. / Meissner, J.W. / Nicolas, A.L. / Perry, B.G. / Phillips, D.J. / Pitt, W.R. / Platt, A. / Ratcliffe, A.J. / Sharpe, A. / Tait, L.J.
External linksBioorg. Med. Chem. Lett. / PubMed:17459703
MethodsX-ray diffraction
Resolution2.4 Å
Structure data

PDB-2p33:
Synthesis and SAR of Aminopyrimidines as Novel c-Jun N-Terminal Kinase (JNK) Inhibitors
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

ChemComp-J07:
4-{[5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl]amino}-N-ethylpiperidine-1-carboxamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / JNK3 kinase / inhibitor

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