HDAC4 Inhibitors

Santa Cruz Biotechnology now offers a broad range of HDAC4 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. HDAC4 Inhibitors offered by Santa Cruz inhibit HDAC4 and, in some cases, other chromatin remodeling and transcription regulation related proteins. View detailed HDAC4 Inhibitor specifications, including HDAC4 Inhibitor CAS number, molecular weight, molecular formula and chemical structure, by clicking on the product name.

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PRODUCT NAME/Application CAS Catalog # QUANTITY Price Citations RATING
Trichostatin A
A potent and non-competitive reversible inhibitor of HDAC
58880-19-6 sc-3511
1 mg
5 mg
KD 5170
An HDAC1, HDAC2, HDAC3, HDAC4, and HDAC6 inhibitor
940943-37-3 sc-362755
10 mg
MC 1568
A class II (IIa) HDAC inhibitor selective for HDAC4 and HDAC6
852475-26-4 sc-362767
10 mg
50 mg
An HDAC1, HDAC2, HDAC4, HDAC10, and HDAC11 inhibitor
875320-29-9 sc-364515
5 mg
50 mg
An HDAC1, HDAC2, HDAC4, and HDAC6 inhibitor
128517-07-7 sc-364603
1 mg
5 mg
LMK 235
An HDAC4 and HDAC5 inhibitor
1418033-25-6 sc-397051
5 mg
25 mg

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