JIB-04
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- Application
- Inhibition (Inh)
- Fonction
- pan-JUMONJI histone demethylase inhibitor
- Attributs du produit
- A novel specific inhibitor of the Jumonji family of histone demethylases in vitro, in cancer cells and in tumors in vivo. IC50 = 230, 340, 435, 445, 855 and 1100 nM for JARID1A, JMJD2E, JMJD2B, JMJD2A, JMJD3 and JMJD2C respectively. Reduces tumor burden and prolongs life in a mouse model. Suppresses translation initiation and enhances mTOR inhibitor sensitivity. Inhibits the growth of temozolomide-resistant glioblastoma cells and crosses the blood brain barrier.
- Pureté
- >98 %
- Chemical Name
- (E)-5-Chloro-2-(2-(phenyl(pyridine-2-yl)methylene)hydrazinyl)pyridine
- Formula
- C17H13ClN4
- Perméabilité
- Cell-permeable
- Solubility
- Soluble in DMSO (up to 30 mg/ml).
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- Restrictions
- For Research Use only
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- Format
- Powder
- Stock
- -20 °C
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- Sujet
- Epigenetics,Posttranslational modification,Protein demethylase,Cancer,mTOR,Chromatin
- Poids moléculaire
- 308.76
- Numéro CAS
- 199596-05-9
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