Trichostatin A

Pricing Availability   Qty
Description: Potent histone deacetylase inhibitor
Chemical Name: (2E,4E,6R)-7-(4-(Dimethylamino)phenyl)-N-hydroxy-4,6-dimethyl-7-oxo-2,4-heptadienamide
Purity: ≥95% (HPLC)
Datasheet
Citations (8)
Reviews (1)
Literature (2)

Biological Activity for Trichostatin A

Trichostatin A is a selective and potent inhibitor of class I and II histone deacetylases (HDAC) (Ki = 3.4 nM, IC50 values are 4.99 nM, 5.21 nM, 16.4 nM, 24.3 nM, 27.6 nM for HDAC1, 3, 6, 10 and 4, respectively). Trichostatin A induces accelerated dedifferentiation of primordial germ cells (PGCs) into embryonic germ (EG) cells. Trichostatin A potently inhibits a range of breast cancer and melanoma cell lines (IC50 = 29-400 nM) and induces apoptosis in prostate cancer cells. In an animal model of Huntington's disease, inhibition of HDAC by Trichostatin A rescues memory deficits and increases expression of CREB/CBP target genes in mutant mice. Activates autophagy, increases vesicular transport of BDNF (Cat. No. 2837) and is active in vivo.Trichostatin A enhances CRISPR-Cas9 gene editing of human induced pluripotent stem cells (iPSCs).

Technical Data for Trichostatin A

M. Wt 302.37
Formula C17H22N2O3
Storage Store at -20°C
Purity ≥95% (HPLC)
CAS Number 58880-19-6
PubChem ID 444732
InChI Key RTKIYFITIVXBLE-QEQCGCAPSA-N
Smiles O=C([C@H](C)/C=C(C)/C=C/C(NO)=O)C1=CC=C(N(C)C)C=C1

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

Tocris products are intended for laboratory research use only, unless stated otherwise.

Solubility Data for Trichostatin A

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 5 17

Preparing Stock Solutions for Trichostatin A

The following data is based on the product molecular weight 302.37. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.17 mM 19.45 mL 97.27 mL 194.54 mL
0.85 mM 3.89 mL 19.45 mL 38.91 mL
1.7 mM 1.95 mL 9.73 mL 19.45 mL
8.5 mM 0.39 mL 1.95 mL 3.89 mL

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Product Datasheets for Trichostatin A

Certificate of Analysis / Product Datasheet
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References for Trichostatin A

References are publications that support the biological activity of the product.

Durcova-Hills et al (2008) Reprogramming primordial germ cells into pluripotent stem cells. PloS ONE 3 e3531 PMID: 18953407

Yoshida et al (1990) Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A. J.Biol.Chem. 265 17174 PMID: 2211619

Vigushin et al (2001) Trichostatin A is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo. Clin.Cancer Res. 7 971 PMID: 11309348

Wharton et al (2000) Inhibition of mitogenesis in Balb/c-3T3 cells by trichostatin A. J.Biol.Chem. 275 33981 PMID: 10945992

Galluzzi et al (2017) Pharmacological modulation of autophagy: therapeutic potential and persisting obstacles. Nat.Rev.Drug.Discov. PMID: 28529316

Tatamiya et al (2004) Isozyme-selective activity of the HDAC inhibitor MS-275. Proc.Amer.Assoc.Cancer Res. 45

Giralt et al (2012) Long-term memory deficits in Huntington's disease are associated with reduced CBP histone acetylase activity. Hum.Mol.Genet. 21 1203 PMID: 22116937

Molugu et al (2023) Trichostatin A for efficient CRISPR-Cas9 gene editing of human pluripotent stem cells. CRISPR J. 6 473 PMID: 37676985


If you know of a relevant reference for Trichostatin A, please let us know.

View Related Products by Product Action

View all Non-selective Histone Deacetylase Inhibitors

Keywords: Trichostatin A, Trichostatin A supplier, Histone, deacetylase, inhibitors, inhibits, HDAC, Deacetylases, TrichostatinA, stem, cells, epigenetics, cancer, melanoma, apoptosis, Huntingtons, autophagy, BDNF, CRISPR, Cas9, reagents, iPSCs, Stem, Cell, Reprogramming, Autophagy, Non-selective, HDACs, Non-Selective, Reagents, 1406, Tocris Bioscience

8 Citations for Trichostatin A

Citations are publications that use Tocris products. Selected citations for Trichostatin A include:

Parira et al (2019) Trichostatin A Shows Transient Protection from Chronic Alcohol-Induced Reactive Oxygen Species (ROS) Production in Human Monocyte-Derived Dendritic Cells. J Alcohol Drug Depend 6 PMID: 30596124

Xia et al (2013) Identification of repurposed small molecule drugs for chordoma therapy. Cancer Biol Ther 14 638 PMID: 23792643

Kurita et al (2012) HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity. Nat Neurosci 15 1245 PMID: 22864611

Lu et al (2019) Histone deacetylase 4 promotes type I IF. signaling, restricts DNA viruses, and is degraded via vaccinia virus protein C6. Proc Natl Acad Sci U S A PMID: 31127039


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Reviews for Trichostatin A

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TSA test.
By Yu Chen on 08/21/2024
Assay Type: In Vitro
Species: Human
Cell Line/Tissue: pancreatic tumor

We used TSA for organoid culture to induce cell proliferation that can be detected by Brdu.

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Literature in this Area

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

*Please note that Tocris will only send literature to established scientific business / institute addresses.


Epigenetics Scientific Review

Epigenetics Scientific Review

Written by Susanne Müller-Knapp and Peter J. Brown, this review gives an overview of the development of chemical probes for epigenetic targets, as well as the impact of these tool compounds being made available to the scientific community. In addition, their biological effects are also discussed. Epigenetic compounds available from Tocris are listed.

Rheumatoid Arthritis Poster

Rheumatoid Arthritis Poster

Rheumatoid arthritis (RA) is a chronic destructive inflammatory autoimmune disease that results from a breakdown in immune tolerance, for reasons that are as yet unknown. This poster summarizes the pathology of RA and the inflammatory processes involved, as well as describing some of the epigenetic modifications associated with the disease and the potential for targeting these changes in the discovery of new treatments.