期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 284, 期 19, 页码 12853-12861出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M809430200
关键词
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资金
- National Institutes of Health [U01-NS057153]
- Stanford Synchrotron Radiation Laboratory (SSRL)
- U.S. Dept. of Energy, Office of Basic Energy Sciences
- SSRL Structural Molecular Biology Program
- Dept. of Energy, Office of Biological and Environmental Research
- National Center for Research Resources
- NIH
- Biomedical Technology Program
- NIGMS
c-Jun N-terminal kinase 3 alpha 1 (JNK3 alpha 1) is a mitogen-activated protein kinase family member expressed primarily in the brain that phosphorylates protein transcription factors, including c-Jun and activating transcription factor-2 (ATF-2) upon activation by a variety of stress-based stimuli. In this study, we set out to design JNK3-selective inhibitors that had > 1000-fold selectivity over p38, another closely related mitogen-activated protein kinase family member. To do this we employed traditional medicinal chemistry principles coupled with structure-based drug design. Inhibitors from the aminopyrazole class, such as SR-3576, were found to be very potent JNK3 inhibitors (IC50 = 7 nM) with > 2800-fold selectivity over p38 (p38 IC50 > 20 mu M) and had cell-based potency of similar to 1 mu M. In contrast, indazole-based inhibitors exemplified by SR-3737 were potent inhibitors of both JNK3 (IC50 = 12 nM) and p38 (IC50 = 3 nM). These selectivity differences between the indazole class and the aminopyrazole class came despite nearly identical binding (root mean square deviation = 0.33 angstrom) of these two compound classes to JNK3. The structural features within the compounds giving rise to the selectivity in the aminopyrazole class include the highly planar nature of the pyrazole, N-linked phenyl structures, which better occupied the smaller active site of JNK3 compared with the larger active site of p38.
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