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TitleSynthesis and SAR of piperazine amides as novel c-jun N-terminal kinase (JNK) inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 19, Page 3344-3347, Year 2009
Publish dateJan 15, 2009 (structure data deposition date)
AuthorsShin, Y. / Chen, W. / Habel, J. / Duckett, D. / Ling, Y.Y. / Koenig, M. / He, Y. / Vojkovsky, T. / LoGrasso, P. / Kamenecka, T.M.
External linksBioorg. Med. Chem. Lett. / PubMed:19433357
MethodsX-ray diffraction
Resolution2.28 Å
Structure data

PDB-3fv8:
JNK3 bound to piperazine amide inhibitor, SR2774.
Method: X-RAY DIFFRACTION / Resolution: 2.28 Å

Chemicals

ChemComp-JK3:
5-bromo-N-(3-chloro-2-(4-(prop-2-ynyl)piperazin-1-yl)phenyl)furan-2-carboxamide

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / JNK3 / protein-inhibitor complex / Alternative splicing / ATP-binding / Chromosomal rearrangement / Cytoplasm / Epilepsy / Kinase / Nucleotide-binding / Phosphoprotein / Serine/threonine-protein kinase

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