An HDAC inhibitor
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Labeled Version(s)
22107SAHA-d5
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SAHA

Item No. 10009929

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
N1-hydroxy-N8-phenyl-octanediamide
CAS Number
149647-78-9
Synonyms
  • Suberoylanilide Hydroxamic Acid
  • Vorinostat
Molecular Formula
C14H20N2O3
Formula Weight
264.3
Purity
≥98%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 20 mg/mlDMSO: 20 mg/mlDMSO:PBS (pH 7.2) (1:1): 0.5 mg/mlEthanol: 0.25 mg/ml
λmax
243 nm
SMILES
ONC(=O)CCCCCCC(=O)Nc1ccccc1
InChi Code
InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18)
InChi Key
WAEXFXRVDQXREF-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    100 mg

    $53

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    250 mg

    $106

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    500 mg

    $198

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    1 g

    $370

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    Product Description

    SAHA is a histone deacetylase (HDAC) inhibitor that binds directly to the catalytic site of the enzyme thereby blocking substrate access. It inhibits class I, II, and IV HDACs at 50-200 nM and arrests cell growth in a wide variety of transformed cells in culture at 2.5-5.0 µM.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Marks, P.A., and Breslow, R. Dimethyl sulfoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug. Nat. Biotechnol. 25(1), 84-90 (2007).

    Product Citations

    Villoria-González, A., Zierfuss, B., Parzer, P., et al. Efficacy of HDAC inhibitors in driving peroxisomal β-oxidation and immune responses in human macrophages: Implications for neuroinflammatory disorders. Biomolecules 13(12), 1696 (2023).

    Shim, G., Han, S.-E., Yu, Y.-H., et al. Trilysinoyl oleylamide-based cationic liposomes for systemic co-delivery of siRNA and an anticancer drug. J. Control. Release 155(1), 60-66 (2011).