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Title5-Ureidobenzofuranone indoles as potent and efficacious inhibitors of PI3 kinase-alpha and mTOR for the treatment of breast cancer.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 20, Page 3526-3529, Year 2010
Publish dateApr 13, 2010 (structure data deposition date)
AuthorsZhang, N. / Ayral-Kaloustian, S. / Anderson, J.T. / Nguyen, T. / Das, S. / Venkatesan, A.M. / Brooijmans, N. / Lucas, J. / Yu, K. / Hollander, I. / Mallon, R.
External linksBioorg. Med. Chem. Lett. / PubMed:20483602
MethodsX-ray diffraction
Resolution2.87 Å
Structure data

PDB-3mjw:
PI3 Kinase gamma with a benzofuranone inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.87 Å

Chemicals

ChemComp-WYF:
(2Z)-4,6-dihydroxy-2-[(8-methoxy-1,2,3,4-tetrahydropyrazino[1,2-a]indol-10-yl)methylidene]-1-benzofuran-3(2H)-one

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / ATP-binding / Kinase / Nucleotide-binding

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