Scriptaid
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- Application
- Inhibition (Inh)
- Purpose
- HDAC inhibitor
- Characteristics
- 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.
- Purity
- >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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- Restrictions
- For Research Use only
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- Format
- Powder
- Storage
- RT
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- Background
- Scriptide, GCK1026,Proliferation,Epigenetics,Cell cycle,Protein deacetylase,Stem cells,Cancer,Posttranslational modification,Chromatin
- Molecular Weight
- 326.35
- CAS-No
- 287383-59-9
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