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TitleAminopyridine-Based c-Jun N-Terminal Kinase Inhibitors with Cellular Activity and Minimal Cross-Kinase Activity.
Journal, issue, pagesJ. Med. Chem., Vol. 49, Page 3563-3580, Year 2006
Publish dateApr 7, 2006 (structure data deposition date)
AuthorsSzczepankiewicz, B.G. / Kosogof, C. / Nelson, L.T. / Liu, G. / Liu, B. / Zhao, H. / Serby, M.D. / Xin, Z. / Liu, M. / Gum, R.J. ...Szczepankiewicz, B.G. / Kosogof, C. / Nelson, L.T. / Liu, G. / Liu, B. / Zhao, H. / Serby, M.D. / Xin, Z. / Liu, M. / Gum, R.J. / Haasch, D.L. / Wang, S. / Clampit, J.E. / Johnson, E.F. / Lubben, T.H. / Stashko, M.A. / Olejniczak, E.T. / Sun, C. / Dorwin, S.A. / Haskins, K. / Abad-Zapatero, C. / Fry, E.H. / Hutchins, C.W. / Sham, H.L. / Rondinone, C.M. / Trevillyan, J.M.
External linksJ. Med. Chem. / PubMed:16759099
MethodsX-ray diffraction
Resolution3.5 Å
Structure data

PDB-2gmx:
Selective Aminopyridine-Based C-Jun N-terminal Kinase inhibitors with cellular activity
Method: X-RAY DIFFRACTION / Resolution: 3.5 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-877:
N-(4-AMINO-5-CYANO-6-ETHOXYPYRIDIN-2-YL)-2-(4-BROMO-2,5-DIMETHOXYPHENYL)ACETAMIDE

Source
  • homo sapiens (human)
KeywordsTRANSCRIPTION / JNK1 / c-jun N-Terminal Kinase / Protein Kinase Jnk1 inhibitors / Aminopyridine-Based c-Jun N-Terminal Kinase Inhibitors

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