5-Fluoroimidazo[4,5-b]pyridine Is a Privileged Fragment That Conveys Bioavailability to Potent Trypanosomal Methionyl-tRNA Synthetase Inhibitors

نویسندگان

  • Zhongsheng Zhang
  • Cho Yeow Koh
  • Ranae M. Ranade
  • Sayaka Shibata
  • J. Robert Gillespie
  • Matthew A. Hulverson
  • Wenlin Huang
  • Jasmine Nguyen
  • Nagendar Pendem
  • Michael H. Gelb
  • Christophe L. M. J. Verlinde
  • Wim G. J. Hol
  • Frederick S. Buckner
  • Erkang Fan
چکیده

Fluorination is a well-known strategy for improving the bioavailability of drug molecules. However, its impact on efficacy is not easily predicted. On the basis of inhibitor-bound protein crystal structures, we found a beneficial fluorination spot for inhibitors targeting methionyl-tRNA synthetase of Trypanosoma brucei. In particular, incorporating 5-fluoroimidazo[4,5-b]pyridine into inhibitors leads to central nervous system bioavailability and maintained or even improved efficacy.

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عنوان ژورنال:

دوره 2  شماره 

صفحات  -

تاریخ انتشار 2016