ESE-1 Activators are a class of compounds that enhance the functional activity of ESE-1 by acting on various cellular mechanisms. Forskolin, through the increase of cAMP, activates PKA which can phosphorylate and influence the transcriptional activity of ESE-1. This phosphorylation may enhance the binding of ESE-1 to DNA, facilitating its transcriptional efficacy. Epigallocatechin gallate and 5-Aza-2'-deoxycytidine reduce methylation of the ESE-1 promoter region, which may lead to augmented ESE-1 expression and subsequent transcriptional activity. Similarly, Sulforaphane, Trichostatin A, and Sodium butyrate, as HDAC inhibitors, increase histone acetylation, allowing for a more open chromatin structure and improved ESE-1 access to DNA, which enhances its transcriptional regulation capabilities.
Further, Retinoic acid can induce the expression of genes that act as co-factors or enhancers of ESE-1 activity, while Curcumin, by inhibiting NF-κB signaling, can reduce suppressive inflammatory signaling pathways that hinder ESE-1 activity. Resveratrol, through SIRT1 activation, can lead to deacetylation of histones and transcription factors, creating a conducive chromatin environment for ESE-1. Piceatannol and SP600125, by modulating kinase activities, indirectly influence the transcriptional programs that ESE-1 is a part of, enhancing its transcriptional output. Lithium chloride's inhibition of GSK-3 may also contribute to the stabilization of transcription factors or co-activators that enhance ESE-1's transcriptional activity.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | ¥857.00 ¥1692.00 ¥8179.00 ¥15626.00 ¥23128.00 | 73 | |
腺苷酸环化酶激活剂,可增加细胞内cAMP水平,从而激活蛋白激酶A(PKA),通过促进磷酸化反应和随后的转录激活来增强ESE-1活性。 | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | ¥474.00 ¥812.00 ¥1399.00 ¥2685.00 ¥5867.00 ¥13922.00 | 11 | |
多酚可抑制 DNA 甲基转移酶,减少某些基因启动子的甲基化,通过提高 ESE-1 与 DNA 的可及性,增强 ESE-1 的活性。 | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-207495A sc-207495B sc-207495C sc-207495 sc-207495E sc-207495D | 5 mg 10 mg 25 mg 1 g 10 g 250 mg | ¥1692.00 ¥3227.00 ¥5404.00 ¥14655.00 ¥93629.00 ¥10323.00 | 22 | |
HDAC 抑制因子可导致乙酰化程度更高、更开放的染色质结构,从而有可能增强 ESE-1 与目标 DNA 序列的结合及其转录物活性。 | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | ¥733.00 ¥3599.00 ¥6487.00 ¥11259.00 | 28 | |
视黄酸受体的激活剂,可上调基因表达;可通过增加提供辅助因子或促进ESE-1 DNA结合和功能的基因的表达来增强ESE-1的活性。 | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | ¥406.00 ¥767.00 ¥1207.00 ¥2414.00 ¥2640.00 ¥9725.00 ¥22203.00 | 47 | |
NF-kB 信号转导的抑制因子,可能导致对 ESE-1 功能所需的共激活因子的竞争减少,从而增强 ESE-1 的转录物活性。 | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | ¥677.00 ¥2087.00 ¥4118.00 | 64 | |
SIRT1 激活剂,可使组蛋白和转录因子去乙酰化,可能通过调节染色质状态和转录因子的相互作用来增强 ESE-1 的活性。 | ||||||
Piceatannol | 10083-24-6 | sc-200610 sc-200610A sc-200610B | 1 mg 5 mg 25 mg | ¥564.00 ¥790.00 ¥2200.00 | 11 | |
Syk 抑制因子,可改变信号通路,导致转录物发生变化,包括上调与 ESE-1 协同作用的基因,增强其功能活性。 | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | ¥1681.00 ¥5303.00 ¥6995.00 ¥13527.00 ¥23579.00 | 33 | |
HDAC 抑制剂,可增加组蛋白的乙酰化,通过改善 ESE-1 与其目的基因的可及性,从而增强 ESE-1 的活性。 | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | ¥2414.00 | ||
GSK-3 抑制剂可导致 β-catenin 的稳定,从而与 ESE-1 相互作用并增强其转录活性。 | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | ¥2414.00 ¥3565.00 ¥4716.00 | 7 | |
DNA 甲基转移酶抑制剂,可减少 DNA 甲基化,通过增加 ESE-1 或其辅助因子的基因表达,增强 ESE-1 的活性。 |