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A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
Published on: December 7, 2014
Fragment-based discovery of JAK-2 inhibitors
Stephen Antonysamy1, Gavin Hirst, Frances Park
1Medicinal Chemistry, SGX Pharmaceuticals, Inc, San Diego, CA 92121, USA.
Bioorganic & Medicinal Chemistry Letters
|November 21, 2008
Abstract:
Fragment-based hit identification coupled with crystallographically enabled structure-based drug design was used to design potent inhibitors of JAK-2. After two iterations from fragment 1, we were able to increase potency by greater than 500-fold to provide sulfonamide 13, a 78-nM JAK-2 inhibitor.
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