| Literature DB >> 26710088 |
Tom E McAllister1,2, Katherine S England3,4, Richard J Hopkinson1, Paul E Brennan3,4, Akane Kawamura1,2, Christopher J Schofield1.
Abstract
There is increasing interest in targeting histone N-methyl-lysine demethylases (KDMs) with small molecules both for the generation of probes for target exploration and for therapeutic purposes. Here we update on previous reviews on the inhibition of the lysine-specific demethylases (LSDs or KDM1s) and JmjC families of N-methyl-lysine demethylases (JmjC KDMs, KDM2-7), focusing on the academic and patent literature from 2014 to date. We also highlight recent biochemical, biological, and structural studies which are relevant to KDM inhibitor development.Entities:
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Year: 2016 PMID: 26710088 DOI: 10.1021/acs.jmedchem.5b01758
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446