5-Azacytidine
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- Application
- Inhibition (Inh)
- Fonction
- DNA hypomethylation agent
- Attributs du produit
- Specific inhibitor of DNA methyltransferase. Incorporates into DNA and covalently reacts with and inhibits DNA methyltransferases. Induces demethylation and reactivation of silenced genes. Increases stem cell reprogramming efficiency. Induces cardiac differentiation of human mesenchymal stem cells by activating ERK. Induces apoptosis in multiple myeloma cells via ATR-mediated DNA double strand breaks. Cell permeable.
- Pureté
- >98 %
- Chemical Name
- 4-Amino-1-ß-D-ribofuranosyl-1,3,5-triazin-2(1H)-one
- Formula
- C8H12N4O5
- Perméabilité
- Cell-permeable
- Solubility
- Soluble in DMSO (up to 25 mg/ml), or in Water (up to 12 mg/ml).
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- Restrictions
- For Research Use only
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- Format
- Powder
- Précaution d'utilisation
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GHS – Classification
Acute toxicity, Oral (Category 4), H302
Germ cell mutagenicity (Category 2), H341
Carcinogenicity (Category 1A), H350
Reproductive toxicity (Category 1B), H360
Specific target organ toxicity - repeated exposure (Category 1), H372
Long-term (chronic) aquatic hazard (Category 1), H410 - Stock
- -20 °C
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- Sujet
- Ladakamycin, U-18496, NSC-102816, AzaC,Epigenetics,Chromatin,DNA methyltransferase,Stem cells,Cell death,Infectious disease,Apoptosis inducer,DNA damage
- Poids moléculaire
- 244.2
- Numéro CAS
- 320-67-2
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