1. Cell Cycle/DNA Damage Epigenetics Apoptosis
  2. HDAC Caspase Bcl-2 Family
  3. AN-7

AN-7 是一种具有口服活性的组蛋白去乙酰化酶 (HDAC) 抑制剂,在体外和体内诱导组蛋白过度乙酰化和分化,抑制人前列腺 22Rv1 癌细胞的增殖。AN-7 能够增加促凋亡蛋白 Bax 的表达,降低抗凋亡蛋白 Bcl-2 的表达,并通过激活 caspase-3 来促进细胞凋亡 (apoptosis),可用于前列腺癌的研究。

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AN-7 Chemical Structure

AN-7 Chemical Structure

CAS No. : 213262-83-0

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

AN-7 is an orally active histone deacetylase (HDAC) inhibitor that induces histone hyperacetylation and differentiation in vitro and in vivo, and inhibits the proliferation of human prostate 22Rv1 cancer cells. AN-7 can increase the expression of the pro-apoptotic protein Bax, reduce the expression of the anti-apoptotic protein Bcl-2, and promote apoptosis by activating caspase-3, and can be used in the study of prostate cancer[1].

分子量

254.22

Formula

C9H19O6P

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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  • 稀释计算器

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质量   浓度   体积   分子量 *
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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

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浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
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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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产品名称:
AN-7
目录号:
HY-117136
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