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TitleDiscovery of a new class of 4-anilinopyrimidines as potent c-Jun N-terminal kinase inhibitors: Synthesis and SAR studies.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 17, Page 668-672, Year 2007
Publish dateOct 24, 2006 (structure data deposition date)
AuthorsLiu, M. / Wang, S. / Clampit, J.E. / Gum, R.J. / Haasch, D.L. / Rondinone, C.M. / Trevillyan, J.M. / Abad-Zapatero, C. / Fry, E.H. / Sham, H.L. / Liu, G.
External linksBioorg. Med. Chem. Lett. / PubMed:17107797
MethodsX-ray diffraction
Resolution3.2 Å
Structure data

PDB-2no3:
Novel 4-anilinopyrimidines as potent JNK1 Inhibitors
Method: X-RAY DIFFRACTION / Resolution: 3.2 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-859:
2-({2-[(3-HYDROXYPHENYL)AMINO]PYRIMIDIN-4-YL}AMINO)BENZAMIDE

Source
  • homo sapiens (human)
KeywordsSIGNALING PROTEIN/INHIBITOR / JNK1 / C-JUN N-TERMINAL KINASE / JNK1 INHIBITORS / ANILINOPYRIMIDINES JNK1 INHIBITORS / SIGNALING PROTEIN-INHIBITOR COMPLEX

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