Date published: 2025-10-10

021-6093-6350

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EZI激活剂

EZI activators, or Enhancer of Zeste Inhibitor activators, are a class of chemical compounds that specifically interact with a family of proteins known as Polycomb-group (PcG) proteins. PcG proteins are involved in the regulation of gene expression through the modification of chromatin structure, which is the complex of DNA and protein found in the nucleus of eukaryotic cells. One of the key components of this protein family is the Enhancer of Zeste homolog 2 (EZH2), which acts as a methyltransferase, transferring methyl groups to histone proteins-the core components around which DNA is wound. This methylation is a critical process in the epigenetic regulation of genes, playing an essential role in the control of gene activation and repression. EZI activators are designed to modulate the activity of EZH2, thereby influencing the methylation status of histones and ultimately affecting the expression pattern of genes.

The molecular design of EZI activators is rooted in the understanding of the enzymatic mechanism of EZH2. By binding to the catalytic site or allosteric sites of EZH2, these activators can modulate the activity of the enzyme. The structure-activity relationship (SAR) of these molecules is an active area of research, focusing on optimizing the interactions between the EZI activators and EZH2 proteins to achieve desired modulation effects. These compounds are often characterized by their ability to influence the tri-methylation state of histone H3 on lysine 27 (H3K27me3), which is a hallmark of EZH2 enzymatic activity. Understanding the precise mechanism by which EZI activators exert their effect on EZH2 involves detailed studies of molecular biology, biochemistry, and structural biology to elucidate the interaction between these small molecules and their target protein at the atomic level.

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Items 1 to 10 of 12 total

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产品名称CAS #产品编号数量价格应用排名

Forskolin

66575-29-9sc-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
(3)

佛司可林能直接刺激腺苷酸环化酶,提高细胞内 cAMP 的水平。升高的 cAMP 会激活 PKA,然后使目标蛋白磷酸化,从而通过磷酸化依赖机制激活 EZI。

IBMX

28822-58-4sc-201188
sc-201188B
sc-201188A
200 mg
500 mg
1 g
¥1794.00
¥3554.00
¥6747.00
34
(1)

IBMX是一种非选择性磷酸二酯酶抑制剂,可防止cAMP分解,从而维持细胞内高水平的这种第二信使。这可以通过维持PKA活性来支持EZI的激活,从而可能磷酸化EZI。

PMA

16561-29-8sc-3576
sc-3576A
sc-3576B
sc-3576C
sc-3576D
1 mg
5 mg
10 mg
25 mg
100 mg
¥451.00
¥1455.00
¥2369.00
¥5528.00
¥10481.00
119
(6)

PMA是一种蛋白激酶C(PKC)的强效激活剂,可参与多种信号转导通路。PKC激活可通过磷酸化相关底物,产生下游效应,提高EZI的激活状态。

(−)-Epigallocatechin Gallate

989-51-5sc-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
(1)

已知 EGCG 可抑制多种蛋白激酶,从而减少负调控磷酸化事件,通过缓解抑制控制机制间接增强 EZI 的活性。

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
¥1365.00
¥4423.00
148
(1)

LY294002 是一种 PI3K 抑制剂,可以调节下游的 AKT 信号转导。抑制 AKT 可导致可能被 AKT 抑制的某些过程或蛋白质的激活,从而可能导致 EZI 的间接激活。

U-0126

109511-58-2sc-222395
sc-222395A
1 mg
5 mg
¥711.00
¥2719.00
136
(2)

U0126 是 MEK1/2 的抑制剂,通过阻断该激酶可影响 MAPK/ERK 通路。这可能会导致信号动态的改变,从而通过影响相关信号网络间接增强 EZI 的活性。

D-erythro-Sphingosine-1-phosphate

26993-30-6sc-201383
sc-201383D
sc-201383A
sc-201383B
sc-201383C
1 mg
2 mg
5 mg
10 mg
25 mg
¥1828.00
¥3565.00
¥6307.00
¥10030.00
¥19100.00
7
(1)

鞘氨醇-1-磷酸是一种生物活性脂质,可激活鞘氨醇-1-磷酸受体,触发细胞内信号级联反应。这会导致信号通路激活,从而间接提高EZI的功能活性。

A23187

52665-69-7sc-3591
sc-3591B
sc-3591A
sc-3591C
1 mg
5 mg
10 mg
25 mg
¥609.00
¥1444.00
¥2245.00
¥3509.00
23
(1)

A23187是一种离子载体,可增加细胞内钙离子浓度,激活钙离子依赖性信号通路。这会导致钙离子信号调节的蛋白质和过程被激活,从而增强EZI的功能活性。

Staurosporine

62996-74-1sc-3510
sc-3510A
sc-3510B
100 µg
1 mg
5 mg
¥925.00
¥1692.00
¥4377.00
113
(4)

Staurosporine是一种广谱蛋白激酶抑制剂,可通过抑制通常抑制某些途径的激酶来选择性激活这些途径,从而间接激活EZI。

Genistein

446-72-0sc-3515
sc-3515A
sc-3515B
sc-3515C
sc-3515D
sc-3515E
sc-3515F
100 mg
500 mg
1 g
5 g
10 g
25 g
100 g
¥293.00
¥1038.00
¥1354.00
¥3497.00
¥5641.00
¥10244.00
¥20545.00
46
(1)

染料木素是一种酪氨酸激酶抑制剂,可通过降低竞争性酪氨酸激酶的活性,缓解竞争性信号传导并增强导致 EZI 激活的途径。