1. Epigenetics
  2. Histone Methyltransferase
  3. E67-2

E67-2 作为 E67 衍生物,是一种低毒、选择性 KIAA1718 Jumonji 结构域抑制剂,其 IC50 值为3.4 µM。E67-2 选择性抑制组蛋白 H3 赖氨酸 9 (H3K9) Jumonji 去甲基化酶,以及组蛋白 H3 赖氨酸 4 (H3K4) 去甲基化酶。

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E67-2 Chemical Structure

E67-2 Chemical Structure

CAS No. : 1364914-62-4

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

E67-2, as the E67 derivative, is a low-toxicity, selective KIAA1718 Jumonji domain inhibitor with an IC50 value of 3.4 µM. E67-2 selectively inhibits histone H3 lysine 9 (H3K9) Jumonji demethylase as well as histone H3 lysine 4 (H3K4) demethylase[1].

IC50 & Target

IC50: 3.4 μM (H3K9 Jumonji demethylase)[1]

体外研究
(In Vitro)

E67-2 (1~100 μM; 5 minutes) reduces inhibitory effect against GLP by a factor of approximately 1500, resulting in an IC50 of 75 µM. E67-2 has much reduced inhibition on PHF8 on the doubly methylated H3(1-24)K4me3K9me2 peptide substrate. E67-2 (100~100000 nM; 24 hours; fibroblasts) has significantly reduced cell toxicity [1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

404.55

Formula

C21H36N6O2

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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E67-2
目录号:
HY-122746
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