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MilliporeSigma™ Calbiochem™ HDAC6 Inhibitor II, BRD9757

Catalog No. 5057600001 Shop All MilliporeSigma Products
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Catalog No. 50-576-00001 Supplier MilliporeSigma™ Supplier No. 5057600001
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A cell-permeable, low molecular weight hydroxamate compound that acts as a potent histone deacetylase class IIb HDAC6-selective inhibitor (IC50 = 30nM), while inhibiting class I HDAC1/2/3/8 only at higher concentrations (IC50

A cell-permeable, low molecular weight hydroxamate compound that acts as a potent histone deacetylase class IIb HDAC6-selective inhibitor (IC50 = 30nM), while inhibiting class I HDAC1/2/3/8 only at higher concentrations (IC50 = 0.638, 1.79, 0.694, and 1.09μM, respectively) and exhibiting much reduced potency against class IIa HDAC4/5/7/9 (IC50 >12.61μM). Shown to selectively upregulate HDAC6 substrate α-tubulin acetylation in HeLa cells (10 and 30μM; 24 h) without inducing histone H3 acetylation increase seen with another HDAC6-selective inhibitor Tubastatin A (Cat. No. 382187). Unlike other Zinc-binding group-containing HDAC inhibitors, BRD9757 does not contain an apparent selectivity-imparting capping structure linked to its hydroxamate.
TRUSTED_SUSTAINABILITY

Specifications

Color Pale Orange
Description 98% by HPLC
Target Proteins HDAC6
Molecular Formula C6H9NO2
Solubility DMSO
Content And Storage Protect from light
Form Solid
Quantity 10 mg
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