Structural basis for the inhibition of Aurora A kinase by a novel class of high affinity disubstituted pyrimidine inhibitors
We have characterized a novel binding mode for a newly discovered 2,4-disubstituted pyrimidine inhibitor of AIK, using X-ray crystallography. This structure provides an excellent basis for the design of specific and potent compounds with potential therapeutic value in the treatment of cancer. The 2....
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2007-02, Vol.17 (3), p.688-691 |
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