1. Cell Cycle/DNA Damage Apoptosis Epigenetics
  2. Sirtuin Apoptosis
  3. Sirt1/2-IN-3

Sirt1/2-IN-3 (compound PS9) 是 SIRT1/2 的双重抑制剂,IC50 分别为 1.4 μM (SIRT1) 和 2.0 μM (SIRT2)。Sirt1/2-IN-3 完全阻断 p53 脱乙酰化,并增加 p53 和 α-微管蛋白乙酰化。 Sirt1/2-IN-3 诱导细胞凋亡并对人白血病细胞系显示出抗增殖活性。

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Sirt1/2-IN-3 Chemical Structure

Sirt1/2-IN-3 Chemical Structure

CAS No. : 301313-42-8

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Sirt1/2-IN-3 (compound PS9) is a dual inhibitor of SIRT1/2 with IC50s of 1.4 μM (SIRT1) and 2.0 μM (SIRT2), respsectivley. Sirt1/2-IN-3 completely blocks p53 deacetylation, and increase of p53 and α-tubulin acetylation. Sirt1/2-IN-3 induces apoptosis and shows anti-proliferation activity against human leukemia cell lines[1].

IC50 & Target

IC50: 1.4 μM (SIRT1), 2.0 μM (SIRT2), 72.3 μM (SIRT3)[1]

体外研究
(In Vitro)

Sirt1/2-IN-3 (compound hsa55) (5 μM; 48 h) 诱导不同肿瘤细胞凋亡,IC50 分别为 6.5 μM (MV4-11)、9.2μM (MOLM-13)、27.2 μM (THP1)、17.4 μM (Jurkat)[1]
Sirt1/2-IN-3 (100 μM; 30 min) 会降低 SIRT1SIRT2 蛋白在不同温度下的热稳定性,并且 (25 μM、30 μM; 24 h) 会增加 MOLM-13 细胞中 p53 和 α 微管蛋白乙酰化形式的水平[1]

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

分子量

363.82

Formula

C17H14ClNO4S

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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    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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HY-155728
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