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Boosting NAD+ with a small molecule that activates NAMPT.

Stephen J GardellMeghan HopfAsima KhanMauro DispagnaE Hampton SessionsRebecca FalterNidhi KapoorJeanne BrooksJeffrey CulverChris PetucciChen-Ting MaSteven E CohenJun TanakaEmmanuel S BurgosJennifer S HirschiSteven R SmithEduard SergienkoAnthony B Pinkerton
Published in: Nature communications (2019)
Pharmacological strategies that boost intracellular NAD+ are highly coveted for their therapeutic potential. One approach is activation of nicotinamide phosphoribosyltransferase (NAMPT) to increase production of nicotinamide mononucleotide (NMN), the predominant NAD+ precursor in mammalian cells. A high-throughput screen for NAMPT activators and hit-to-lead campaign yielded SBI-797812, a compound that is structurally similar to active-site directed NAMPT inhibitors and blocks binding of these inhibitors to NAMPT. SBI-797812 shifts the NAMPT reaction equilibrium towards NMN formation, increases NAMPT affinity for ATP, stabilizes phosphorylated NAMPT at His247, promotes consumption of the pyrophosphate by-product, and blunts feedback inhibition by NAD+. These effects of SBI-797812 turn NAMPT into a "super catalyst" that more efficiently generates NMN. Treatment of cultured cells with SBI-797812 increases intracellular NMN and NAD+. Dosing of mice with SBI-797812 elevates liver NAD+. Small molecule NAMPT activators such as SBI-797812 are a pioneering approach to raise intracellular NAD+ and realize its associated salutary effects.
Keyphrases
  • small molecule
  • high throughput
  • reactive oxygen species
  • protein protein
  • oxidative stress
  • signaling pathway
  • cell death
  • fluorescent probe
  • single molecule
  • highly efficient