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A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
Published on: December 7, 2014
9H-Carbazole-1-carboxamides as potent and selective JAK2 inhibitors
Kurt Zimmermann1, Xiaopeng Sang1, Harold A Mastalerz1
1Bristol-Myers Squibb Co., 5 Research Parkway, Wallingford, CT 06492-1951, USA.
Abstract:
The discovery, synthesis, and characterization of 9H-carbazole-1-carboxamides as potent and selective ATP-competitive inhibitors of Janus kinase 2 (JAK2) are discussed. Optimization for JAK family selectivity led to compounds 14 and 21, with greater than 45-fold selectivity for JAK2 over all other members of the JAK kinase family.
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