1. Epigenetics
  2. Histone Demethylase
  3. S1427

S1427 是一种反苯环丙胺衍生的 LSD1 抑制剂,IC50 为 390 nM,Ki 为 80 nM。S1427 抑制 hERG 通道,且具有微粒体稳定性。抑制 LSD1 可减少癌细胞的增殖。

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S1427 Chemical Structure

S1427 Chemical Structure

CAS No. : 2447061-40-5

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查看 Histone Demethylase 亚型特异性产品:

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生物活性

S1427 is a tranylcypromine-derived LSD1 inhibitor with the IC50 of 390 nM and Ki of 80 nM. S1427 exhibits desirable hERG channel inhibition and microsomal stability profiles. Inhibition of LSD1 partially reduces the proliferation of cancer cells[1].

IC50 & Target

KDM1/LSD1

 

分子量

474.52

Formula

C25H29F3N4O2

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

S1427 相关分类

  • 摩尔计算器

  • 稀释计算器

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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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:
S1427
目录号:
HY-146380
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