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647925  Trichostatin A, Streptomyces sp.

4,6-Dimethyl-7-[p-dimethylaminophenyl]-7-oxahepta-2,4-dienohydroxamic Acid, TSA

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19 May 2013

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647925-1MG  1 mg 
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A potent and reversible, cell-permeable inhibitor of histone deacetylase. Blocks cell cycle progression at the G1 phase in HeLa cells and induces a 12-fold increase in intracellular levels of gelsolin. Induces reversion of oncogenic ras-transformed NIH/3T3 cells to a normal morphology. Inhibits IL-2 gene expression (IC50 = 73 nM) in Jurkat cells and shows immunosuppressive activity in a mouse model. Down-regulates p57kip2 in Hep 3B cells. A 10 mM (500 µg/165 µl) solution of Trichostatin A, Streptomyces sp. (Cat. No. 647926) in DMSO is also available.
Product information
Form Off-white lyophilized solid
Primary Target histone deactylase
Secondary target IL-2 gene expression (IC50 = 73 nM)
Molar mass 302.4
Cell permeable Yes
Reversible Yes
Purity ≥98% by HPLC
Solubility DMSO, EtOH, MeOH
Chemical formula C17H22N2O3
RTECS MI5215000
CAS number 58880-19-6
Store and ship information
Storage -20°C
Ship Ambient Temperature Only
Harmful
Safety information
S Phrase S: 26-36

In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
Wear suitable protective clothing.
R Phrase R: 20/21/22-36/37/38-43

Harmful by inhalation, in contact with skin and if swallowed.
Irritating to eyes, respiratory system and skin.
May cause sensitization by skin contact.
Trichostatin A, <i>Streptomyces </i>sp., molecular structure

© Merck KGaA, Darmstadt, Germany, 2013

All references to Merck refer to Merck KGaA, Darmstadt, Germany.


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