Optimisation of a triazolopyridine based histone demethylase inhibitor yields a potent and selective KDM2A (FBXL11) inhibitor†

نویسندگان

  • Katherine S. England
  • Anthony Tumber
  • Tobias Krojer
  • Giuseppe Scozzafava
  • Stanley S. Ng
  • Michelle Daniel
  • Aleksandra Szykowska
  • KaHing Che
  • Frank von Delft
  • Nicola A. Burgess-Brown
  • Akane Kawamura
  • Christopher J. Schofield
  • Paul E. Brennan
چکیده

A potent inhibitor of the JmjC histone lysine demethylase KDM2A (compound 35, pIC50 7.2) with excellent selectivity over representatives from other KDM subfamilies has been developed; the discovery that a triazolopyridine compound binds to the active site of JmjC KDMs was followed by optimisation of the triazole substituent for KDM2A inhibition and selectivity.

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عنوان ژورنال:

دوره 5  شماره 

صفحات  -

تاریخ انتشار 2014