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TitlePotent and Selective Aurora Inhibitors Identified by the Expansion of a Novel Scaffold for Protein Kinase Inhibition.
Journal, issue, pagesJ. Med. Chem., Vol. 48, Page 3080-, Year 2005
Publish dateMar 11, 2005 (structure data deposition date)
AuthorsFancelli, D. / Berta, D. / Bindi, S. / Cameron, A. / Cappella, P. / Carpinelli, P. / Catana, C. / Forte, B. / Giordano, P. / Giorgini, M.L. ...Fancelli, D. / Berta, D. / Bindi, S. / Cameron, A. / Cappella, P. / Carpinelli, P. / Catana, C. / Forte, B. / Giordano, P. / Giorgini, M.L. / Mantegani, S. / Marsiglio, A. / Meroni, M. / Moll, J. / Pittala, V. / Roletto, F. / Severino, D. / Soncini, C. / Storici, P. / Tonani, R. / Varasi, M. / Vulpetti, A. / Vianello, P.
External linksJ. Med. Chem. / PubMed:15828847
MethodsX-ray diffraction
Resolution2.6 Å
Structure data

PDB-2bmc:
Aurora-2 T287D T288D complexed with PHA-680632
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

Chemicals

ChemComp-MPY:
(3E)-N-(2,6-DIETHYLPHENYL)-3-{[4-(4-METHYLPIPERAZIN-1-YL)BENZOYL]IMINO}PYRROLO[3,4-C]PYRAZOLE-5(3H)-CARBOXAMIDE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / CELL CYCLE / SERINE/THREONINE-PROTEIN KINASE / ATP-BINDING / PHOSPHORYLATION

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