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TitleDiscovery of benzisoxazoles as potent inhibitors of chaperone heat shock protein 90.
Journal, issue, pagesJ. Med. Chem., Vol. 51, Page 373-375, Year 2008
Publish dateDec 12, 2007 (structure data deposition date)
AuthorsGopalsamy, A. / Shi, M. / Golas, J. / Vogan, E. / Jacob, J. / Johnson, M. / Lee, F. / Nilakantan, R. / Petersen, R. / Svenson, K. ...Gopalsamy, A. / Shi, M. / Golas, J. / Vogan, E. / Jacob, J. / Johnson, M. / Lee, F. / Nilakantan, R. / Petersen, R. / Svenson, K. / Chopra, R. / Tam, M.S. / Wen, Y. / Ellingboe, J. / Arndt, K. / Boschelli, F.
External linksJ. Med. Chem. / PubMed:18197612
MethodsX-ray diffraction
Resolution1.6 Å
Structure data

PDB-3bm9:
Discovery of Benzisoxazoles as Potent Inhibitors of Chaperone Hsp90
Method: X-RAY DIFFRACTION / Resolution: 1.6 Å

PDB-3bmy:
Discovery of Benzisoxazoles as Potent Inhibitors of Chaperone Hsp90
Method: X-RAY DIFFRACTION / Resolution: 1.6 Å

Chemicals

ChemComp-BXZ:
4-bromo-6-(6-hydroxy-1,2-benzisoxazol-3-yl)benzene-1,3-diol

ChemComp-HOH:
WATER

ChemComp-CXZ:
4-chloro-6-{5-[(2-morpholin-4-ylethyl)amino]-1,2-benzisoxazol-3-yl}benzene-1,3-diol

Source
  • homo sapiens (human)
KeywordsCHAPERONE / ATP binding domain / Alternative splicing / ATP-binding / Cytoplasm / Nucleotide-binding / Phosphoprotein / Stress response

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