Date published: 2025-10-11

021-6093-6350

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UNR激活剂

NADK activators constitute a distinctive class of chemical compounds that possess the unique ability to enhance the activity or expression of NAD kinase (NADK), an enzyme intricately involved in the cellular regulation of nicotinamide adenine dinucleotide (NAD+). NAD+ stands as a pivotal coenzyme that exerts indispensable roles in diverse biological processes, including energy metabolism, DNA repair, and cellular signaling. The emergence of NADK activators has garnered substantial attention due to their potential to modulate NAD+ levels, thereby influencing downstream cellular functions. These activators can encompass a diverse array of chemical structures, yet they commonly share the property of augmenting NADK's activity through direct or indirect mechanisms. Some activators function by increasing the availability of NAD+ precursors, such as nicotinamide riboside (NR) or nicotinamide mononucleotide (NMN). These precursors serve as substrates for NAD+ synthesis, thereby facilitating the elevation of cellular NAD+ levels, which can lead to subsequent NADK activation. Additionally, NADK activators may target intracellular signaling pathways, such as those involving AMP-activated protein kinase (AMPK) or sirtuins, ultimately culminating in the modulation of NAD+ metabolism. These compounds often act as triggers, initiating a cascade of events that collectively contribute to the augmentation of NADK's enzymatic activity.

As our understanding of the intricate web of cellular processes continues to evolve, NADK activators hold significant promise as tools for investigating the fundamental roles of NAD+ in various physiological contexts. By enabling the manipulation of NADK activity, these compounds provide a means to explore the intricate interplay between NAD+ homeostasis and cellular functions, shedding light on the underlying mechanisms that govern vital biological processes. While not yet fully characterized in terms of their broader implications, NADK activators stand as promising entities that could potentially uncover novel insights into cellular regulatory networks and contribute to our comprehension of the intricate molecular choreography that sustains cellular life.

関連項目

产品名称CAS #产品编号数量价格应用排名

Actinomycin D

50-76-0sc-200906
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sc-200906B
sc-200906C
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放线菌素 D 是一种抗生素,可通过与 DNA 结合抑制转录。通过阻止 RNA 合成,它间接影响了 UNR。UNR 的调控功能通常依赖于它与特定 RNA 分子的相互作用。放线菌素 D 可破坏这些 RNA 靶标的转录,改变它们与 UNR 结合的可用性,从而调节其调控作用。

Cordycepin

73-03-0sc-203902
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(1)

虫草素是一种核苷类似物,可在转录过程中与 RNA 结合。通过干扰 RNA 合成,虫草素间接影响了 UNR。它有可能影响 UNR 与之相互作用的 RNA 分子的稳定性和处理过程,从而影响其在转录后基因调控中的调控作用。

Rapamycin

53123-88-9sc-3504
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$62.00
$155.00
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233
(4)

雷帕霉素是一种免疫抑制剂,可抑制 mTOR(哺乳动物雷帕霉素靶标)通路,这是翻译的一个关键调节因子。雷帕霉素可通过改变翻译率间接调节 UNR 的活性。UNR 参与翻译调节,而雷帕霉素对 mTOR 的抑制可影响 UNR 对 mRNA 翻译的作用。

Cycloheximide

66-81-9sc-3508B
sc-3508
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127
(5)

环己亚胺是一种蛋白质合成抑制剂,可影响翻译速率。它通过改变新生多肽的可用性和翻译速度间接影响 UNR 的功能。UNR 在翻译调节中的作用会受到蛋白质合成动态变化的影响。

Leptomycin B

87081-35-4sc-358688
sc-358688A
sc-358688B
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35
(2)

Leptomycin B 是一种核输出抑制剂,可干扰 RNA 和蛋白质从细胞核输出到细胞质。通过干扰 RNA 定位过程,Leptomycin B 间接影响了 UNR。UNR 参与 mRNA 定位,改变 RNA 分子在细胞内的迁移会影响其调控功能。