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TitleThe Discovery of furo[2,3-c]pyridine-based indanone oximes as potent and selective B-Raf inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 21, Page 1248-1252, Year 2011
Publish dateDec 1, 2010 (structure data deposition date)
AuthorsBuckmelter, A.J. / Ren, L. / Laird, E.R. / Rast, B. / Miknis, G. / Wenglowsky, S. / Schlachter, S. / Welch, M. / Tarlton, E. / Grina, J. ...Buckmelter, A.J. / Ren, L. / Laird, E.R. / Rast, B. / Miknis, G. / Wenglowsky, S. / Schlachter, S. / Welch, M. / Tarlton, E. / Grina, J. / Lyssikatos, J. / Brandhuber, B.J. / Morales, T. / Randolph, N. / Vigers, G. / Martinson, M. / Callejo, M.
External linksBioorg. Med. Chem. Lett. / PubMed:21211972
MethodsX-ray diffraction
Resolution3.4 Å
Structure data

PDB-3psb:
Furo[2,3-c]pyridine-based Indanone Oximes as Potent and Selective B-Raf Inhibitors
Method: X-RAY DIFFRACTION / Resolution: 3.4 Å

Chemicals

ChemComp-SM6:
ethyl 3-{[1-(hydroxyamino)-2H-inden-5-yl]amino}thieno[2,3-c]pyridine-2-carboxylate

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / Kinase / ATP-binding / Cardiomyopathy / Disease mutation / Metal-binding / Nucleotide-binding / Phorbol-ester binding / Phosphoprotein / Proto-oncogene / Serine/threonine-protein kinase / Zinc-finger / TRANSFERASE-TRANSFERASE INHIBITOR complex

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