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Trichostatin A - ≥98%, high purity , CAS No.58880-19-6, Inhibitor of histone deacetylase 1;Inhibitor of histone deacetylase 2;Inhibitor of histone deacetylase 3;Inhibitor of histone deacetylase 4;Inhibitor of histone deacetylase 5;Inhibitor of histone deacetylase 6;Inhibitor of histone deacetylase 7;Inhibitor

  • Moligand™
  • ≥98%
Item Number
T129665
Grouped product items
SKUSizeAvailabilityPrice Qty
T129665-1mg
1mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$68.90
T129665-5mg
5mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$286.90
T129665-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$464.90
T129665-25mg
25mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$929.90
T129665-50mg
50mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,484.90

Potent, selective histone deacetylase inhibitor

Basic Description

Synonymstrichostatin A|58880-19-6|TSA|Trichostatin A (TSA)|Trichostatin|(2E,4E,6R)-7-[4-(Dimethylamino)phenyl]-N-hydroxy-4,6-dimethyl-7-oxohepta-2,4-dienamide|Antibiotic A-300|(R)-Trichostatin A|CHEBI:46024|C17H22N2O3|(R,2E,4E)-7-(4-(dimethylamino)phenyl)-N-hydro
Specifications & Purity≥98%
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of histone deacetylase 1;Inhibitor of histone deacetylase 2;Inhibitor of histone deacetylase 3;Inhibitor of histone deacetylase 4;Inhibitor of histone deacetylase 5;Inhibitor of histone deacetylase 6;Inhibitor of histone deacetylase 7;Inhibitor
Product Description

Trichostatin A (TSA) is an HDAC inhibitor with IC50 of ~1.8 nM – HDAC8 is the only known member of the HDAC-family that is not affected by TSA.
A potent and non-competitive reversible inhibitor of HDAC.

Associated Targets

HDAC4 Tclin Histone deacetylase 4 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC1 Tclin Histone deacetylase 1 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC7 Tclin Histone deacetylase 7 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC11 Tclin Histone deacetylase 11 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC9 Tclin Histone deacetylase 9 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC2 Tclin Histone deacetylase 2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SF3B3 Tchem Splicing factor 3B subunit 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

F3 Tclin Tissue factor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC10 Tclin Histone deacetylase 10 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC8 Tclin Histone deacetylase 8 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC5 Tclin Histone deacetylase 5 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC3 Tclin Histone deacetylase 3 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name (2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4,6-dimethyl-7-oxohepta-2,4-dienamide
INCHI InChI=1S/C17H22N2O3/c1-12(5-10-16(20)18-22)11-13(2)17(21)14-6-8-15(9-7-14)19(3)4/h5-11,13,22H,1-4H3,(H,18,20)/b10-5+,12-11+/t13-/m1/s1
InChi Key RTKIYFITIVXBLE-QEQCGCAPSA-N
Canonical SMILES CC(C=C(C)C=CC(=O)NO)C(=O)C1=CC=C(C=C1)N(C)C
Isomeric SMILES C[C@H](/C=C(\C)/C=C/C(=O)NO)C(=O)C1=CC=C(C=C1)N(C)C
WGK Germany 3
RTECS MI5215000
PubChem CID 444732
Molecular Weight 302.37
Reaxy-Rn 2391788

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

12 results found

Lot NumberCertificate TypeDateItem
K2212414Certificate of AnalysisAug 21, 2024 T129665
E2325536Certificate of AnalysisApr 27, 2023 T129665
E2325540Certificate of AnalysisApr 27, 2023 T129665
E2325546Certificate of AnalysisApr 27, 2023 T129665
E2325550Certificate of AnalysisApr 27, 2023 T129665
E2325553Certificate of AnalysisApr 27, 2023 T129665
H2304161Certificate of AnalysisApr 27, 2023 T129665
H2201090Certificate of AnalysisAug 08, 2022 T129665
G2221294Certificate of AnalysisJul 23, 2022 T129665
G2405045Certificate of AnalysisJun 15, 2022 T129665
K2212408Certificate of AnalysisJun 15, 2022 T129665
K2212410Certificate of AnalysisJun 15, 2022 T129665

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Chemical and Physical Properties

SolubilitySoluble in water (Partly Miscible), ethanol (2 mg/mL), DMSO (20 mg/mL), acetonitrile, DMF (30 mg/mL), and methanol
SensitivityHeat sensitive
Specific Rotation[α]136° (C=0.3,MeOH)
Melt Point(°C)144 °C(dec.)

Safety and Hazards(GHS)

Pictogram(s) GHS07
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H302:Harmful if swallowed

H317:May cause an allergic skin reaction

H312:Harmful in contact with skin

H332:Harmful if inhaled

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

WGK Germany 3
RTECS MI5215000
Reaxy-Rn 2391788
Merck Index 9649

Related Documents

References

1. Bradner JE, West N, Grachan ML, Greenberg EF, Haggarty SJ, Warnow T, Mazitschek R.  (2010)  Chemical phylogenetics of histone deacetylases..  Nat Chem Biol,  (3): (238-243).  [PMID:20139990]
2. Gehring KB et al..  (2016)  Involvement of phosphorylated Apis mellifera CREB in gating a honeybee's behavioral response to an external stimulus..  Learn Mem,  23  (5): (195-207).  [PMID:27084927]
3. Wang Y et al..  (2019)  Dexmedetomidine attenuates the toxicity of ß-amyloid on neurons and astrocytes by increasing BDNF production under the regulation of HDAC2 and HDAC5..  Mol Med Rep,  19  (533-540).  [PMID:30483749]
4. Hu JX et al..  (2022)  Macrophage migration inhibitory factor (MIF) acetylation protects neurons from ischemic injury..  Cell Death Dis,  13  (5): (466).  [PMID:35585040]

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