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19 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
26710088 248 Recent Progress in Histone Demethylase Inhibitors.EBI University of Oxford
26771107 113 Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 1. 3-Amino-4-pyridine Carboxylate Derivatives.EBI GlaxoSmithKline R&D
26741168 239 8-Substituted Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives As Potent, Cell Permeable, KDM4 (JMJD2) and KDM5 (JARID1) Histone Lysine Demethylase Inhibitors.EBI The Institute of Cancer Research
26771203 114 Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives.EBI GlaxoSmithKline R&D
26491978 24 Novel 5-carboxy-8-HQ based histone demethylase JMJD2A inhibitors: introduction of an additional carboxyl group at the C-2 position of quinoline.EBI China Pharmaceutical University
24971742 4 KDM4B as a target for prostate cancer: structural analysis and selective inhibition by a novel inhibitor.EBI National Tsing-Hua University
23964788 56 Identification of the KDM2/7 histone lysine demethylase subfamily inhibitor and its antiproliferative activity.EBI Kyoto Prefectural University of Medicine
23725560 22 Quantitative analysis of histone demethylase probes using fluorescence polarization.EBI University of Colorado
23587423 1 A small molecule inhibitor of fungal histone acetyltransferase Rtt109.EBI University of Massachusetts Medical School
22975593 62 Oncoepigenomics: making histone lysine methylation count.EBI TBA
21955276 60 Lysine demethylases inhibitors.EBI Kyoto Prefectural University of Medicine
20684604 46 Design, synthesis, enzyme-inhibitory activity, and effect on human cancer cells of a novel series of jumonji domain-containing protein 2 histone demethylase inhibitors.EBI Nagoya City University
20088513 8 Selective inhibitors of the JMJD2 histone demethylases: combined nondenaturing mass spectrometric screening and crystallographic approaches.EBI University of Oxford
28262558 62 Potent and Selective KDM5 Inhibitor Stops Cellular Demethylation of H3K4me3 at Transcription Start Sites and Proliferation of MM1S Myeloma Cells.BDB University of Oxford