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TitleDesign and synthesis of 2-amino-isoxazolopyridines as Polo-like kinase inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 18, Page 5186-5189, Year 2008
Publish dateMay 30, 2008 (structure data deposition date)
AuthorsHanan, E.J. / Fucini, R.V. / Romanowski, M.J. / Elling, R.A. / Lew, W. / Purkey, H.E. / VanderPorten, E.C. / Yang, W.
External linksBioorg. Med. Chem. Lett. / PubMed:18790636
MethodsX-ray diffraction
Resolution3.15 Å
Structure data

PDB-3db8:
Crystal structure of an activated (Thr->Asp) Polo-like kinase 1 (Plk1) catalytic domain in complex with Compound 041
Method: X-RAY DIFFRACTION / Resolution: 3.15 Å

Chemicals

ChemComp-1FR:
3-[3-chloro-5-(5-{[(1S)-1-phenylethyl]amino}isoxazolo[5,4-c]pyridin-3-yl)phenyl]propan-1-ol

Source
  • danio rerio (zebrafish)
KeywordsTRANSFERASE / Polo-like kinase 1 / Plk1 / catalytic domain / small-molecule inhibitor / Kinase

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