Santa Cruz Biotechnology now offers a broad range of HDAC8 Inhibitors. Histone deacetylase proteins (HDACs) are a class of enzymes that remove acetyl groups (O=C-CH3) from an <ε>-N-acetyl lysine amino acid on a histone, allowing histones to wrap DNA more tightly. The deacetylation of histones is associated with transcriptional silencing. Histone deacetylase inhibitors (HDIs) have a long history of use in psychiatry and neurology as mood stabilizers and anti-epileptic. HDIs are studied as a treatment for neurodegenerative diseases and have a potential for cancer therapy. HDAC8 Inhibitors offered by Santa Cruz inhibit HDAC8 and, in some cases, other chromatin remodeling and transcription regulation related proteins. View detailed HDAC8 Inhibitor specifications, including HDAC8 Inhibitor CAS number, molecular weight, molecular formula and chemical structure, by clicking on the product name.
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