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TitleImidazo[5,1-f][1,2,4]triazin-2-amines as novel inhibitors of polo-like kinase 1.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 18, Page 6214-6217, Year 2008
Publish dateSep 26, 2008 (structure data deposition date)
AuthorsCheung, M. / Kuntz, K.W. / Pobanz, M. / Salovich, J.M. / Wilson, B.J. / Andrews, C.W. / Shewchuk, L.M. / Epperly, A.H. / Hassler, D.F. / Leesnitzer, M.A. ...Cheung, M. / Kuntz, K.W. / Pobanz, M. / Salovich, J.M. / Wilson, B.J. / Andrews, C.W. / Shewchuk, L.M. / Epperly, A.H. / Hassler, D.F. / Leesnitzer, M.A. / Smith, J.L. / Smith, G.K. / Lansing, T.J. / Mook, R.A.
External linksBioorg. Med. Chem. Lett. / PubMed:18929484
MethodsX-ray diffraction
Resolution3.2 Å
Structure data

PDB-3eoc:
Cdk2/CyclinA complexed with a imidazo triazin-2-amine
Method: X-RAY DIFFRACTION / Resolution: 3.2 Å

Chemicals

ChemComp-T2A:
5-methyl-7-phenyl-N-(3,4,5-trimethoxyphenyl)imidazo[5,1-f][1,2,4]triazin-2-amine

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/CELL CYCLE / cdk / cyclin / ATP-binding / Cell cycle / Cell division / Kinase / Mitosis / Nucleotide-binding / Phosphoprotein / Serine/threonine-protein kinase / Transferase / Nucleus / TRANSFERASE-CELL CYCLE COMPLEX

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