Inhibitors of bcr-abl... Breaking new ground again

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The report of a new class of potent and highly selective inhibitors of Bcr-abl highlights the potential for a truly leukemia-specific drug with no expected off-target activity. GNF-2, as a


representative compound of this class, may have inspired the identification of a region of Bcr-abl that is amenable to drug design, just as imatinib did almost a decade ago. Access through


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_Curr. Opin. Drug Discov._ 8, 487–494 (2005). CAS  Google Scholar  Download references ACKNOWLEDGEMENTS The authors would like to thank Dick Leopold for his thoughtful review of the


manuscript and Chris Faehnjle for his assistance in the preparation of the figure. AUTHOR INFORMATION Author notes * Jeffrey F. Ohren and Judith S. Leopold: Jeffrey F. Ohren is in Chemical


Technologies and Judith S. Leopold is in Mechanistic and Target Biology AUTHORS AND AFFILIATIONS * Ann Arbor Laboratories, Pfizer Global Research and Development, Ann Arbor, 48105, Michigan,


USA Jeffrey F Ohren & Judith S Sebolt-Leopold Authors * Jeffrey F Ohren View author publications You can also search for this author inPubMed Google Scholar * Judith S Sebolt-Leopold


View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Ohren, J.,


Sebolt-Leopold, J. Inhibitors of Bcr-abl... breaking new ground again. _Nat Chem Biol_ 2, 63–64 (2006). https://doi.org/10.1038/nchembio0206-63 Download citation * Issue Date: February 2006


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