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| N-(2-Aminophenyl)-N'-phenylheptanediamide Basic information |
| N-(2-Aminophenyl)-N'-phenylheptanediamide Chemical Properties |
Melting point | 159-161°C | Boiling point | 627.9±40.0 °C(Predicted) | density | 1.212±0.06 g/cm3(Predicted) | storage temp. | -20°C Freezer | solubility | DMSO, Methanol | form | Beige solid | pka | 14?+-.0.70(Predicted) | color | Off-White to Pale Beige |
| N-(2-Aminophenyl)-N'-phenylheptanediamide Usage And Synthesis |
Chemical Properties | Off-White Solid | Uses | Histone deacetylase inhibitor IV. A cell-permeable pimeloylanilide compound that acts as a FXN-(frataxin gene) specific HDAC inhibitor. Reverses the silencing of FXN transcription in FRDA (Friedrich’s ataxia) cells due to hypoacetylation of histones H3 and H4. | General Description | A cell-permeable pimeloylanilide compound that acts as a FXN- (frataxin gene) specific HDAC (histone deacetylase) inhibitor. Reverses the silencing of FXN transcription in FRDA (Friedreich′s ataxia) cells (~3-fold increase of FXN mRNA at 5 μM in primary FRDA lymphocytes and ~3-fold frataxin expression in FRDA cell line at 2.5 μM) due to hypoacetylation of histones H3 and H4 by increasing acetylation at H3K14, H4K5 and H4K12, without significant changes in acetylation at H3K9, H4K8 and H4K16. In comparison, Trichostatin-A (Cat. No. 647925 and 647926) and SAHA, two other commonly used HDAC inhibitors, exhibit no effect on FXN transcription. | Biochem/physiol Actions | Cell permeable: yes |
| N-(2-Aminophenyl)-N'-phenylheptanediamide Preparation Products And Raw materials |
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