Cat. No. 4652
Alternative Name: Vorinostat
Chemical Name: N-Hydroxy-N'-phenyloctanediamide
Biological ActivityInhibits Class I and II histone deacetylases (HDACs); induces accumulation of acetylated histones H2A, H2B, H3 and H4 in transformed cultured cells. Suppresses cell growth in a range of cancer cell lines; induces apoptosis in cutaneous T cell lymphoma cells in vitro.
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Certificate of Analysis / Product Datasheet / Safety Datasheet
References are publications that support the products' biological activity.
Huangfu et al (2008) Induction of pluripotent stem cells by defined factors is greatly improved by small-molecule compounds. Nat.Biotechnol. 26 795. PMID: 18568017.
Marks and Breslow (2007) Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug. Nat.Biotechnol. 25 84. PMID: 17211407.
Leoni et al (2002) The antitumor histone deacetylase inhibitor suberoylanilide hydroxamic acid exhibits antiinflammatory properties via suppression of cytokines. Proc.Natl.Acad.Sci.U.S.A 99 2995. PMID: 11867742.
Butler et al (2000) Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res. 60 5165. PMID: 11016644.
If you know of a relevant reference for SAHA please let us know.
Citations are publications that use Tocris products. Selected citations for SAHA include:
Sarenac et al (2016) Single-cell analysis reveals IGF-1 potentiation of inhibition of the TGF-β/Smad pathway of fibrosis in humankeratocytes in vitro Scientific Reports 6 34373. PMID: 27687492.
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Keywords: SAHA, supplier, histone, deacetylases, HDACs, inhibits, inhibitors, Class, I, Class, II, vorinostat, anticancer, antiproliferatives, epigenetics, proapoptotic, Tocris Bioscience, Histone Deacetylase Inhibitor products
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