Trichostatin A (TSA)

CAS No. 58880-19-6

Trichostatin A (TSA)( (TSA) )

Catalog No. M15172 CAS No. 58880-19-6

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.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 101 In Stock
5MG 177 In Stock
10MG 336 In Stock
25MG 470 In Stock
50MG 680 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Trichostatin A (TSA)
  • Note
    Research use only, not for human use.
  • Brief 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.
  • 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.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    (TSA)
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    58880-19-6
  • Formula Weight
    302.4
  • Molecular Formula
    C17H22N2O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:23 mg/mL (76.05 mM); Ethanol:<1 mg/mL (<1 mM); Water:<1 mg/mL (<1 mM)
  • SMILES
    C[C@H](/C=C(\C)/C=C/C(=O)NO)C(=O)C1=CC=C(C=C1)N(C)C
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Vigushin DM, et al. Clin Y Res, 2001, 7(4), 971-976.
molnova catalog
related products
  • MC-1568

    A potent and selective class IIa HDAC inhibitor with IC50 of 220 nM for maize HD1-A.

  • MPT0E028

    MPT0E028 (MPT 0E028) is a potent HDAC inhibitor that inhibits nuclear HDAC activity with IC50 of 11.1 nM in HeLa cells.

  • Droxinostat

    Droxinostat (NS-41080) is a selective HDAC inhibitor with IC50 of 16.9, 2.47 and 1.46 uM for HDAC3, HDAC6 and HDAC8, respectively.