Nature Communications · 2019 · 160 citations · 22 references
Life SciencesMedicinal ChemistryPharmacologyCellular MetabolismDrug DiscoveryMolecular PharmacologyEnzyme InhibitionNicotinamide Adenine Dinucleotide MetabolismProtein PhosphorylationActive Site InhibitorsNicotinamide Adenine Dinucleotide (Nad+) MetabolismNicotinamide Adenine Dinucleotide BiosynthesisNicotinamide Mononucleotide AdenylyltransferaseNicotinamide Mononucleotide MetabolismNicotinamide PhosphoribosyltransferaseNicotinic Acid PhosphoribosyltransferaseSmall-molecule Activators
Abstract 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.
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Role of poly(ADP-ribose) formation in DNA repair
Masahiko S. Satoh, Tomas Lindahl · Nature · 1992 · 1.2K citations