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TitleSynthesis, Biological Evaluation, X-ray Structure, and Pharmacokinetics of Aminopyrimidine c-jun-N-terminal Kinase (JNK) Inhibitors
Journal, issue, pagesJ. Med. Chem., Vol. 53, Page 419-431, Year 2010
Publish dateNov 30, 2009 (structure data deposition date)
AuthorsKamenecka, T. / Jiang, R. / Song, X. / Duckett, D. / Chen, W. / Ling, Y.Y. / Habel, J. / Laughlin, J.D. / Chambers, J. / Figuera-Losada, M. ...Kamenecka, T. / Jiang, R. / Song, X. / Duckett, D. / Chen, W. / Ling, Y.Y. / Habel, J. / Laughlin, J.D. / Chambers, J. / Figuera-Losada, M. / Cameron, M.D. / Lin, L. / Ruiz, C.H. / Lograsso, P.V.
External linksJ. Med. Chem. / PubMed:19947601
MethodsX-ray diffraction
Resolution2.4 Å
Structure data

PDB-3kvx:
JNK3 bound to aminopyrimidine inhibitor, SR-3562
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

ChemComp-FMY:
N-[(2Z)-4-(3-fluoro-5-morpholin-4-ylphenyl)pyrimidin-2(1H)-ylidene]-4-(3-morpholin-4-yl-1H-1,2,4-triazol-1-yl)aniline

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / JNK3 / MAPK10 / inhibitor / ATP-binding / Epilepsy / Kinase / Nucleotide-binding / Phosphoprotein / Serine/threonine-protein kinase

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