Tranylcypromine hemisulfate (±)
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- Application
- Inhibition (Inh)
- Fonction
- Demethylase inhibitor
- Attributs du produit
- Irreversible inhibitor of lysine-specific demethylase 1 (LSD1/BHC110) IC50 < 2 μM. Tranylcypromine treatment of P19 embryonal carcinoma cells resulted in global increase of H3K4 methylation along with transcriptional derepression of two BHC110 target genes, Egr1 and Oct4. When combined with CHIR99021, induces the generation of human-induced pluripotent stem cells in the absence of exogenous Sox2. Reduces proliferation, cell cycle progression and invasiveness of endometriotic stromal cells. Upregulates CD86 expression in THP1 cells. Monoamine oxidase inhibitor. Cell permeable and active in vivo.
- Pureté
- >98 %
- Chemical Name
- Trans (±)-2-phenylcyclopropanamine, hemisulfate salt
- Formula
- C9H11N 1/2(H2SO4)
- Perméabilité
- Cell-permeable
- Solubility
- Soluble in Water (up to 25 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
- 2-PCPA, SKF-385,Epigenetics,Protein demethylase,Monoamine oxidase,Stem cells,Neuroscience,Mood disorders,Chromatin,Posttranslational Modification
- Poids moléculaire
- 182.23
- Numéro CAS
- 13492-01-8
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