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TitleIdentification and structure-activity relationship of 2-morpholino 6-(3-hydroxyphenyl) pyrimidines, a class of potent and selective PI3 kinase inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 20, Page 6895-6898, Year 2010
Publish dateOct 1, 2010 (structure data deposition date)
AuthorsPecchi, S. / Renhowe, P.A. / Taylor, C. / Kaufman, S. / Merritt, H. / Wiesmann, M. / Shoemaker, K.R. / Knapp, M.S. / Ornelas, E. / Hendrickson, T.F. ...Pecchi, S. / Renhowe, P.A. / Taylor, C. / Kaufman, S. / Merritt, H. / Wiesmann, M. / Shoemaker, K.R. / Knapp, M.S. / Ornelas, E. / Hendrickson, T.F. / Fantl, W. / Voliva, C.F.
External linksBioorg. Med. Chem. Lett. / PubMed:21035331
MethodsX-ray diffraction
Resolution3.2 Å
Structure data

PDB-3p2b:
Crystal Structure of PI3K gamma with 3-(2-morpholino-6-(pyridin-3-ylamino)pyrimidin-4-yl)phenol
Method: X-RAY DIFFRACTION / Resolution: 3.2 Å

Chemicals

ChemComp-P2B:
3-[2-morpholin-4-yl-6-(pyridin-3-ylamino)pyrimidin-4-yl]phenol

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / PI3-kinase p110 subunit gamma / Transferase / Lipid Kinase / ATP Binding / TRANSFERASE-TRANSFERASE INHIBITOR complex

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