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
1 mL x 10 mM in DMSO 174 In Stock
2MG 106 In Stock
5MG 187 In Stock
10MG 354 In Stock
25MG 496 In Stock
50MG 702 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
  • BRD4354

    BRD4354 is a moderately potent, selective, reversible inhibitor of HDAC5 and HDAC9 with IC50 of 0.85 uM and 1.88 uM.

  • Exifone

    Exifone is a mixed, nonessential activator of HDAC1 that is capable of binding to both free and substrate-bound enzyme, resulting in an increased relative maximal rate of HDAC1-catalyzed deacetylation.

  • Encorafenib

    LGX818 is an orally available mutated BRaf V600E inhibitor(IC50=0.3 nM) with potential antineoplastic activity.