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TitleDesign and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 15, Page 5095-5099, Year 2005
Publish dateSep 16, 2005 (structure data deposition date)
AuthorsSwahn, B.M. / Huerta, F. / Kallin, E. / Malmstrom, J. / Weigelt, T. / Viklund, J. / Womack, P. / Xue, Y. / Ohberg, L.
External linksBioorg. Med. Chem. Lett. / PubMed:16140012
MethodsX-ray diffraction
Resolution1.9 Å
Structure data

PDB-2b1p:
inhibitor complex of JNK3
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-AIZ:
3-{6-[(2-CHLOROPHENYL)AMINO]-1H-INDAZOL-3-YL}-5-{[4-(DIMETHYLAMINO)BUTANOYL]AMINO}BENZOIC ACID

ChemComp-BME:
BETA-MERCAPTOETHANOL

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / enzyme-inhibitor complex / kinase inhibitor

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