Analyzed the data: JZ
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Inhibitors like FK866 and CHS828, which are based on heterocyclic structures and act by binding to the active site of NAMPT 215,216 , are being investigated for their potential to selectively target cancer cells by exploiting their high NAD + turnover 214
Moro J, Tom D, Schmidely P, Demersay T-C, Azzout-Marniche D
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