England, Katherine S <br/><br/>
Optimisation of a triazolopyridine based histone demethylase inhibitor yields a potent and selective KDM2A (FBXL11) inhibitor.  [electronic resource] 

 -  MedChemComm  Dec 2014 
 - 1879-1886 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>2040-2503 
<br/><br/><label>Standard No.: </label>10.1039/C4MD00291A  doi