Potent,selective, cell permeable yeast NAD+-dependent HDAC Sir2p inhibitor
Potent, selective and cell permeable yeast NAD+-dependent histone deacetylase (HDAC) Sir2p inhibitor. Displays higher activity in vivo than in vitro. Sensitizes mammalian cells to a variety of DNA-damaging agents by abrogating Sir2p activity on p53. Acts by either altering or blocking access to the acetylated histone binding pocket. Shown to have diverse effects also in mammalian cells.
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