Inhibition of the histone demethylase JMJD2E by 3-substituted pyridine 2,4-dicarboxylates.
Based on structural analysis of the human 2-oxoglutarate (2OG) dependent JMJD2 histone N(ε)-methyl lysyl demethylase family, 3-substituted pyridine 2,4-dicarboxylic acids were identified as potential inhibitors with possible selectivity over other human 2OG oxygenases. Microwave-assisted palladium-c...
المؤلفون الرئيسيون: | Thalhammer, A, Mecinović, J, Loenarz, C, Tumber, A, Rose, N, Heightman, T, Schofield, C |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2011
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مواد مشابهة
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Inhibition of the histone demethylase JMJD2E by 3-substituted pyridine 2,4-dicarboxylates.
حسب: Thalhammer, A, وآخرون
منشور في: (2011) -
Zn-ejection for the selective inhibition of JMJD2 histone demethylases
حسب: Sekirnik, R, وآخرون
منشور في: (2012) -
Inhibition of the histone lysine demethylase JMJD2A by ejection of structural Zn(II).
حسب: Sekirnik, R, وآخرون
منشور في: (2009) -
Selective inhibitors of the JMJD2 histone demethylases: combined nondenaturing mass spectrometric screening and crystallographic approaches.
حسب: Rose, N, وآخرون
منشور في: (2010) -
Selective inhibitors of the JMJD2 histone demethylases: combined nondenaturing mass spectrometric screening and crystallographic approaches.
حسب: Rose, N, وآخرون
منشور في: (2010)