19 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
26710088	248	Recent Progress in Histone Demethylase Inhibitors.	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.	Glaxosmithkline
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.	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.	Glaxosmithkline
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.	China Pharmaceutical University
24971742	4	KDM4B as a target for prostate cancer: structural analysis and selective inhibition by a novel inhibitor.	National Tsing Hua University
23964788	56	Identification of the KDM2/7 histone lysine demethylase subfamily inhibitor and its antiproliferative activity.	Kyoto Prefectural University of Medicine
23725560	22	Quantitative analysis of histone demethylase probes using fluorescence polarization.	University of Colorado
23587423	1	A small molecule inhibitor of fungal histone acetyltransferase Rtt109.	University of Massachusetts Medical School
22975593	62	Oncoepigenomics: making histone lysine methylation count.	TBA
21955276	60	Lysine demethylases inhibitors.	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.	Nagoya City University
20088513	8	Selective inhibitors of the JMJD2 histone demethylases: combined nondenaturing mass spectrometric screening and crystallographic approaches.	University of Oxford
	12	Calorimetric Studies on the Complexation of Several Ferrocene Derivatives by .alpha.- and .beta.-Cyclodextrin. Effects of Urea on the Thermodynamic Parameters	University of Miami
19237286	30	Design of potent thiophene inhibitors of polo-like kinase 1 with improved solubility and reduced protein binding.	Gsk
19260677	11	Structure-activity relationships of orotidine-5'-monophosphate decarboxylase inhibitors as anticancer agents.	Toronto General Research Institute
18729351	21	Potent cationic inhibitors of West Nile virus NS2B/NS3 protease with serum stability, cell permeability and antiviral activity.	University of Queensland
28841282	2	Synthetic Lethality Triggered by Combining Olaparib with BRCA2-Rad51 Disruptors.	Istituto Italiano Di Tecnologia