1. Cell Cycle/DNA Damage Epigenetics
  2. HDAC
  3. HDAC6-IN-66

HDAC6-IN-66 是一种强效且选择性的组蛋白去乙酰化酶 (HDAC) 6 抑制剂,其 IC50 值为 1.2 nM。HDAC6-IN-66 诱导 α-微管蛋白乙酰化的作用强于组蛋白 H3。HDAC6-IN-66 可用于癌症相关研究。

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HDAC6-IN-66

HDAC6-IN-66 Chemical Structure

CAS No. : 3095060-23-1

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

HDAC6-IN-66 is a potent and selective histone deacetylase (HDAC) 6 inhibitor with an IC50 of 1.8 nM. HDAC6-IN-66 induces α-tubulin acetylation over histone H3. HDAC6-IN-66 can be used for the research of cancer[1].

IC50 & Target[1]

HDAC6

1.8 nM (IC50)

HDAC3

73.6 nM (IC50)

HDAC1

104.9 nM (IC50)

体外研究
(In Vitro)

HDAC6-IN-66 (Compound 5j) 可选择性抑制 HDAC6 (IC50 值为 1.8 nM),对其他 HDAC 亚型的 IC50 显著更高 (HDAC1:104.9 nM,HDAC3:73.6 nM;HDAC4:271.3 nM)[1]
HDAC6-IN-66 对 HCT116 细胞表现出显著的抗增殖活性 (GI50 值为 3.1 μM),对其他癌细胞系如 MDA-MB-231 (GI50 值为 22.3 μM) 和 HCC827 细胞(GI50 值为 15.9 μM) 则显示出温和的抑制活性[1]
HDAC6-IN-66 (0.5-10 μM, 24 h) 可诱导 HCT116 和 MDA-MB-231 细胞中 α-微管蛋白的乙酰化[1]

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

分子量

333.34

Formula

C19H15N3O3

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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  • 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:
HDAC6-IN-66
目录号:
HY-178333
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