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Boosting NAD+ with a small molecule that activates NAMPT

机译:用激活命名的小分子提升NAD +

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Pharmacological strategies that boost intracellular NADsup+/sup are highly?coveted for their therapeutic potential. One approach is activation of nicotinamide phosphoribosyltransferase (NAMPT) to increase production of nicotinamide mononucleotide (NMN), the predominant NADsup+/sup 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 NADsup+/sup. 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 NADsup+/sup. Dosing of mice with SBI-797812 elevates liver NADsup+/sup. Small molecule NAMPT activators such as SBI-797812 are a pioneering approach to raise intracellular NADsup+/sup and realize its associated salutary effects.
机译:促进细胞内NAD + 的药理策略非常垂涎,用于其治疗潜力。一种方法是烟氨基酰胺磷基三烷基(Nampt)的激活,以增加哺乳动物细胞中的烟酰胺酰胺单核苷酸(NMN)的产量,主要的NAD + 前体。用于命名激活器和击球运动的高吞吐量筛选SBI-797812,一种化合物,其在结构上类似于有源点定向的命名抑制剂并阻止这些抑制剂的结合命名。 SBI-797812将Nampt反应平衡转移到NMN形成,增加对ATP的Nampt亲和力,稳定在HIS247处的磷酸化命名,促进氨基磷酸酯的消耗,并通过NAD + 钝化反馈抑制。 SBI-797812的这些效果将命名为“超级催化剂”,其更有效地产生NMN。用SBI-797812处理培养的细胞增加细胞内NMN和NAD + / sup>。用SBI-797812的小鼠给药升高了肝脏NAD + 。 SBI-797812如SBI-797812的小分子命名激活剂是提高细胞内NAD + 的先进方法,并实现其相关的良性效应。

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