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Merck
CN

Boosting NAD+ with a small molecule that activates NAMPT.

Nature communications (2019-07-22)
Stephen J Gardell, Meghan Hopf, Asima Khan, Mauro Dispagna, E Hampton Sessions, Rebecca Falter, Nidhi Kapoor, Jeanne Brooks, Jeffrey Culver, Chris Petucci, Chen-Ting Ma, Steven E Cohen, Jun Tanaka, Emmanuel S Burgos, Jennifer S Hirschi, Steven R Smith, Eduard Sergienko, Anthony B Pinkerton
摘要

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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Sigma-Aldrich
抗-N1-磷酸组氨酸(1-pHis)抗体,克隆SC1-1, clone SC1-1, from rabbit
Sigma-Aldrich
抗乙酰组蛋白H4(Lys16)抗体, Upstate®, from rabbit
Sigma-Aldrich
SBI-797812, ≥98% (HPLC)