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 |
---|---|---|---|---|---|---|
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | ¥338.00 ¥519.00 ¥925.00 ¥2459.00 | 18 | |
HDAC 抑制剂,可导致组蛋白的超乙酰化,通过提高 ESE-1 与其目的基因启动子的可及性,从而增强 ESE-1 的活性。 | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | ¥733.00 ¥3012.00 | 257 | |
能调节 AP-1 活性的 JNK 抑制因子,有可能通过改变与 ESE-1 有相互作用的基因的转录调控来增强 ESE-1 的活性。 |