SS-208

CAS No. 2245942-72-5

SS-208 ( SS208 )

Catalog No. M26826 CAS No. 2245942-72-5

SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 215 Get Quote
10MG 357 Get Quote
25MG 597 Get Quote
50MG 851 Get Quote
100MG 1152 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    SS-208
  • Note
    Research use only, not for human use.
  • Brief Description
    SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.
  • Description
    SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.(In Vivo):In C57BL/6 mice injected immunogenic murine SM1 melanoma cells, SS-208 (25 mg/kg; i.p.) causes a significant reduction of the tumor growth.
  • Synonyms
    SS208
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    5-HT2
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2245942-72-5
  • Formula Weight
    344.2
  • Molecular Formula
    C13H11Cl2N3O4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ONC(=O)c1cc(CCNC(=O)c2ccc(Cl)c(Cl)c2)on1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Gonyou HW, et al. Effects of amperozide and azaperone on aggression and productivity of growing-finishing pigs. J Anim Sci. 1988 Nov;66(11):2856-64.
molnova catalog
related products
  • Resminostat hydrochl...

    A potent inhibitor of HDAC1/3/6 with IC50s of 43-72 nM; induces hyperacetylation of histone H4 and apoptosis in MM cell lines (IC50=2.5-3 uM).

  • Givinostat

    Givinostat hydrochloride monohydrate is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively.

  • BRD4354

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