Scriptaid
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- 应用范围
- Inhibition (Inh)
- 原理
- HDAC inhibitor
- 产品特性
- Inhibits histone deacetylases (HDAC) 1 and 3 (IC50~0.6 μM) and HDAC8 (IC50~1 μM) and is less toxic compared to trichostatin A. Induces cell cycle arrest and epigenetic changes in colon cancer cells. Together with DRB-inhibition of RNA synthesis, scriptaid enhances gene reprogramming in somatic cell nuclear transfer (SCNT) embryos. Increases exercise endurance in mice.
- 纯度
- >98 %
- Chemical Name
- 6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-N-hydroxyhexanamide
- Formula
- C18H18N2O4
- Solubility
- Soluble in DMSO (up to 4 mg/ml)
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- 限制
- 仅限研究用
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- 状态
- Powder
- 储存条件
- RT
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- 背景
- Scriptide, GCK1026,Proliferation,Epigenetics,Cell cycle,Protein deacetylase,Stem cells,Cancer,Posttranslational modification,Chromatin
- 分子量
- 326.35
- CAS-编号
- 287383-59-9
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